1 |
A Balanced Protein Supplement Fortified with Essential Vitamins , Minerals & DHA |
Each 30g contains:
Protein Hydrolysate 20%
DHA 10 %
Pyridoxine Hydrochloride
Cyanocobalamin
Vitamin D3
Folic Acid
Niacinamide
Calcium
(as Dibasic Calcium Phosphate Dihydrate IP)
Manganese Sulphate
Zinc
(as ZincSulphate Heptahydrate IP)
Iron
(as Ferric Ammonium Citrate IP)
Magnesium Oxide
Cupric Sulphate
Chromium
(as Chromium Chloride USP)
Selenium Dioxide Monohydrate
Potassium Chloride
Sodium Chloride
Iodine (as Potassium Iodide IP)
Excipients |
IP
IP
IP
IP
IP
USP
IP
USP
USP
IP
IP |
5 g
25 mg
0.5 mg
1 mcg
100 IU
0.3 mg
15 mg
200 mg
1.5 mcg
1.5 mg
10 mg
4 mg
2.5 mg
25 mcg
20 mcg
5 mg
33 mg
100 mcg
q.s. |
2 |
ABalanced Protein Supplement Fortified with Essential Vitamins & Minerals |
Each 30gmpowder Contains
Whey Protein 30%
Docosa HexaenoicAcid 10 %
Pyridoxine Hydrochloride
Cyanocobalamin
Vitamin D3
Folic Acid
Niacinamide
Calcium
(as Dibasic Calcium Phosphate Dihydrate IP)
Manganese Sulphate
Zinc
(as ZincSulphate Heptahydrate IP)
Iron
(as Ferric Ammonium Citrate IP)
Magnesium Oxide
Cupric Sulphate
Chromium
(as Chromium Chloride USP)
Selenium Dioxide Monohydrate
Potassium Chloride
Sodium Chloride
Iodine
(as Potassium Iodide IP)
Excipients |
IP
IP
IP
IP
IP
USP
IP
USP
USP
IP
IP |
10 g
25 mg
0.5 mg
1 mcg
100 IU
300 mcg
15 mg
200 mg
1.5 mcg
1.5 mg
10 mg
4 mg
2.5 mg
25 mcg
20 mcg
5 mg
33 mg
100 mcg
q.s. |
3 |
Acebrophylline , Terbutaline Sulphate & Guaiphenesin Syrup |
Each 5ml contains :
Acebrophylline
Terbutaline Sulphate
Guaiphenesin
In a flavoured Syrupybase.
Approved Colour Used. |
IP
IP |
50mg
1.25
50mg
q.s. |
4 |
Acebrophylline & Acetylcysteine Tablets |
Each film coated Tablet Contains:
Acebrophylline
Acetylcysteine
Excipients
Approved colour used. |
BP |
100mg
600mg
q.s. |
5 |
Acebrophylline & N- Acetyl L- Cysteine Tablets |
Each film coatedBilayered Tablet Contains:
Acebrophylline
N- Acetyl L-Cysteine
Excipients
Approved colour used |
BP |
100mg
600mg
q.s. |
6 |
Acebrophylline & N- Acetyl L- Cysteine Tablets |
Each film coated Tablet Contains:
Acebrophylline
N- Acetyl L-Cysteine
Excipients
Approved colour used |
BP |
100mg
600mg
q.s. |
7 |
Acebrophylline Capsule |
Each hardgelatin capsule contain:
Acebrophylline
Excipients
Approved colour used in emptycapsule shell |
|
100 mg
q.s |
8 |
Acebrophylline Sustained Release Tablets |
Each film coated sustained release Tablet contains :
Acebrophylline
Excipients
Approved colour used |
|
200mg
q.s. |
9 |
Acebrophylline Sustained Release Tablets |
Each film coated sustained release Tablet contains :
Acebrophylline
Excipients
Approved colour used |
|
200mg
q.s. |
10 |
Aceclofenac & DrotaverineTablets |
Each FilmCoated Tablet Contains:
Aceclofenac
Drotaverine Hydrochloride
Excipients
Colour : ApprovedColour Used |
IP
IP |
100mg
80mg
q.s. |
11 |
Aceclofenac & Paracetamol Suspension |
Each 5ml contains:
Aceclofenac
Paracetamol
In a Flavoured SyrupyBase.
Approved colour used |
IP
IP |
100mg
250mg
q.s. |
12 |
Aceclofenac & Paracetamol Tablets |
Each Uncoated Tablets Contains:
Aceclofenac
Paracetamol
Excipients
Approved colour used |
IP
IP |
100 mg
325 mg
q.s. |
13 |
Aceclofenac & Serratiopeptidase Tablets |
Each film coated Tablet Contains:
Aceclofenac
Serratiopeptidase
(Eq. to enzyme activityof 30000 units of enteric coated
granules)
Excipients
Approved colour used. |
IP
IP |
100mg
15mg
q.s. |
14 |
Aceclofenac & Serratiopeptidase Tablets |
Each filmcoated tablet contain:
Aceclofenac
Serratiopeptidase
( Eq. to enzyme activityof 20000 units of enteric coated
granules)
Excipients
Approved colour used |
IP
IP |
100 mg
10 mg
q.s. |
15 |
Aceclofenac & Thiocolchicoside Tablets |
Each FilmCoated Tablet Contains:
Aceclofenac
Thiocolchicoside
Excipients
Colour : ApprovedColour Used |
IP
IP |
100mg
4mg
q.s. |
16 |
Aceclofenac & Thiocolchicoside Tablets |
Each FilmCoated Tablet Contains:
Aceclofenac
Thiocolchicoside
Excipients
Colour : ApprovedColour Used |
IP
IP |
100mg
8mg
q.s. |
17 |
Aceclofenac along with Linseed oil, Menthol, Methyl Salicylate & Capsaicin |
Composition :-
Aceclofenac
Linseed Oil
Menthol
Methyl Salicyclate
Capsaicin
Banzyl Alcohol (as Preservative)
Gel base |
IP
BP
IP
IP
USP
IP |
1.5%w/w
3%w/w
5%w/w
10%w/w
0.010%w/w
1%w/w
q.s. |
18 |
Aceclofenac Sustained Release Tablets |
Each FilmCoatedTablet Contains:
Aceclofenac
(AsSustained Release)
Excipients
Colour : ApprovedColour Used |
IP |
200mg
q.s. |
19 |
Aceclofenac Tablets |
Each film coated Tablets Contains :
Aceclofenac
Excipients
Approved colour used. |
IP |
100mg
q.s. |
20 |
Aceclofenac, Paracetamol & Chlorzoxazone Tablet |
Each FilmCoatedTablet Contains
Aceclofenac
Paracetamol
Chlorzoxazone
Excipients
Approved colour used |
IP
IP
USP
q.s. |
100 mg
325 mg
250 mg |
21 |
Aceclofenac, Paracetamol & Chlorzoxazone Tablets |
Each Film coated Tablet Contains:
Aceclofenac
Paracetamol
Chlorzoxazone
Excipients
Approved colour used |
IP
IP
USP |
100mg
325mg
500mg
q.s. |
22 |
Aceclofenac, Paracetamol & Chymotrypsin Tablets |
Each Film coatedTabletsContains:
Aceclofenac
Paracetamol
Trypsin Chymotrypsin
50000 Armour unit of enzymaticactivity
(Supplied bya purified concentrate which has specific Trypsin
and chymotrypsin activity in ratio of Approximate six to one)
Excipients
Approved colour used |
IP
IP |
100 mg
325 mg
50000AU
q.s. |
23 |
Aceclofenac, Paracetamol & Serratiopeptidase Tablets |
Each film coatedTablet Contains:
Aceclofenac
Paracetamol
Serratiopeptidase
(Eq. toenzyme activityof 30000 units of enteric coated
granules)
Excipients
Approved Colour Used |
IP
IP
IP |
100mg
325mg
15mg
q.s. |
24 |
Aceclofenac, Paracetamol & Serratiopeptidase Tablets |
Each film coated Tablet Contains:
Aceclofenac
Paracetamol
Serratiopeptidase
(Eq. to 20,000 Serratiopeptidase units)
Excipients
Approved Colour Used. |
IP
IP
IP |
100mg
325mg
10mg
q.s. |
25 |
Aceclofenac, Paracetamol & Thiocolchicoside Tablet |
Each FilmCoatedTablet Contains
Aceclofenac
Paracetamol
Thiocolchicoside
Excipients
Approved colour used |
IP
IP
q.s. |
100 mg
325 mg
4 mg |
26 |
Aceclofenac, Paracetamol & Thiocolchicoside Tablet |
Each Film Coated Tablet Contains
Aceclofenac
Paracetamol
Thiocolchicoside
Excipients
Approved colour used |
IP
IP
q.s. |
100 mg
325 mg
8 mg
q.s. |
27 |
Aceclofenac, Paracetamol Tablets |
Each FilmcoatedTabletsContains:
Aceclofenac
Paracetamol
Excipients
Approved colour used |
IP
IP |
100 mg
325 mg
q.s. |
28 |
Aceclofenac,Par acetamol, Phenylephrine HCL,Cetirizine HCL&Caffeine Tablets |
Each uncoated tablet contains:
Aceclofenac
Paracetamol
Phenylephrine HCL
Cetirizine HCL
Caffeine Anhydrous |
IP
IP
IP
IP
IP |
100mg
325mg
10mg
5mg
25mg
q.s. |
29 |
Aceclofenac,Paracetamol, Caffeine, Phenylephrine HCL& Cetirizine Hydrochloride Tablets |
Each uncoated tablet contains:
Aceclofenac
Paracetamol
Phenylephrine Hydrochloride
Cetirizine Hydrochloride
Caffeine (Anhydrous)
Excipients
Approved colour used |
IP
IP
IP
IP
IP |
100 mg
325 mg
5 mg
10 mg
25 mg
q.s. |
30 |
Acetaminophen, Dextromethorphan, Guaiphenesin, Phenylephrine HCl, Chlorpheniramine Maleate & Menthol Suspension |
Each 5ml Contains :
Acetaminophen
Dextromethorphan Hydrobromide
Guaiphenesin
Phenylephrine Hydrochloride
Chlorpheniramine Maleate
Menthol
In a flavoured Suspension Base
Colour: Sunset Yellow FCF |
USP
BP
BP
BP
BP
BP |
250mg
10mg
50mg
5mg
2mg
1mg
q.s |
31 |
Acetonide Cream |
Fluocinolone Acetonide
In a cream Base |
IP |
0.1 mg
q.s. |
32 |
Aciclovir Cream IP |
Composition :-
Aciclovir
In a cream Base |
IP |
5%w/w
q.s. |
33 |
Aciclovir Dispersible Tablet IP |
Each uncoated tablet contains:
Aciclovir
Excipients
Approved colour used |
IP |
800 mg |
34 |
Aciclovir Tablet IP |
Each uncoated tablet contain:
Aciclovir
Excipients
Approved colour used |
IP |
800 mg
q.s. |
35 |
Acyclovir Dispersible Tablets IP |
Each uncoatedTabletsContains:
Acyclovir
Excipients
Approved colour used |
IP |
400 mg
q.s. |
36 |
Albendazole & Ivermectin suspension |
Each 5 ml contains:
Albendazole
Ivermectin
Flavoured syrupybase |
IP
IP |
200 mg
1.5 mg |
37 |
Albendazole & Ivermectin Tablet |
Each Uncoated tablet contains:
Albendazole
Ivermectin
Excipients
Colour :-Approved colour used |
IP
IP |
400mg
6mg
q.s. |
38 |
Albendazole Oral Suspension IP |
Each ml Contains:
Albendazole
In flavoured Syrupybase
Approved colour used |
IP |
200 mg
q.s. |
39 |
Albendazole Oral Suspension IP |
Each 5ml contains:
Albendazole
Excipients
Approved colour used |
IP |
200mg
q.s. |
40 |
Albendazole Tablet IP |
Each Uncoated Chewable Tablet Contains:-
Albendazole
Excipients
Colour:-Approved Colour used |
IP |
400mg
q.s. |
41 |
Allopurinol Tablets IP |
Each uncoated tablets contains:
Allopurinol
Excipients
Approved colour used |
IP |
100 mg
q.s. |
42 |
Allopurinol Tablets IP |
Each uncoated tablets contains:
Allopurinol
Excipients
Approved colour used |
IP |
300 mg
q.s. |
43 |
Alpha LipoicAcid, Benfotiamine , Multivitamin & Multimineral Capsules |
Each Hard Gelatin CapsuleContains:
Mecobalamin
Alpha LipoicAcid
Benfotiamine
Vitamin B6
Calcium Pantothenate
Folic Acid
Zinc Oxide
Chromium Picolinate
Inositol
Lutein
Excipients
Approved Colour used. |
IP
USP
IP
IP
IP
IP
USP
USP
USP |
1500mcg
100mg
15mg
3mg
25mg
1.5mg
22.5mg
65mcg
10mcg
5mg
q.s. |
44 |
Alpha-Amylase & Papain Syrup |
Each 5ml contains:
Alpha-Amylase
(Bacterial 1:800)
Papain
In a flavoured non-syrupy base
Approved colour used. |
I.P.
I.P. |
100mg
50mg
q.s. |
45 |
Alprazolam Tablets IP |
Each uncoated tablet contains:
Alprazolam
Excipients
Approved colour used |
IP |
0.25 mg
q.s |
46 |
Alprazolam Tablets IP |
Each uncoated tablet contains:
Alprazolam
Excipients
Approved colour used |
IP |
0.5 mg
q.s |
47 |
Aluminium , Magnesium & simethicone oral Suspension IP |
Each 10ml contains :
Aluminiumhydroxide Gel
Equ. to Dried Aluminium Hydroxide Gel
Magnesium Hydroxide Paste
Equ. to Magnesium Hydroxide
Simethicone
In a flavoured Palatable Base
Colour :Erythrosine & Tartrazine |
IP
IP
IP |
250mg
250mg
50mg
q.s |
48 |
Aluminium Hydroxide, Magnesium Hydroxide & Oxetacaine Oral Suspension |
Each 5 ml contains:
Aluminium Hydroxide
(Added Aluminium Hydroxide paste Eq. to dried aluminium
hydroxide gel )
Magnesium Hydroxide
(Added as magnesium Hydroxide Paste)
Oxetacaine
Flavoured palatable base |
IP
IP
IP
BP |
0.291 g
0.380 g
98 mg
10 mg
q.s. |
49 |
Ambroxal Hydrochloride Drops |
Each ml contains:
Ambroxal Hydrochloride
In a flavoured base
Approved colour used |
IP |
7.5mg
q.s. |
50 |
Ambroxal Hydrochloride Syrup |
Each 5ml contains:
Ambroxal Hydrochloride
In a flavoured base
Approved colour used |
IP |
30mg
q.s. |
51 |
Ambroxol HCl , Terbutaline Sulphate, Guaiphenesin and Menthol Syrup |
Each 5ml contains :
Ambroxol Hydrochloride
Terbutaline Sulphate
Guaiphenesin
Menthol
In a flavoured syrupybase.
Approved colour used. |
IP
IP
IP
IP |
15mg
1.5mg
50mg
2.5mg
q.s. |
52 |
Ambroxol HCL, Cetirizine HCL, Phenylephrine HCL, Guaiphenesin & Menthol Syrup |
Each 5ml Contains:
Ambroxol Hydrochloride
Cetirizine Hydrochloride
Phenylephrine Hydrochloride
Guaiphenesin
Menthol
In flavoured Palatable base
Approved colour used |
IP
IP
IP
IP
IP |
4 mg
2.5 mg
5 mg
50 mg
1 mg
q.s. |
53 |
Ambroxol HCl, Levosalbutamol & Guaiphenesin Drops |
Each ml Contains :
Ambroxol Hydrochloride
Levosalbutamol Sulphate
Equ. to Levosalbutamol
Guaiphenesin
In a Flavoured SyrupyBase
Colour : Ponceau 4R |
IP
IP
IP |
7.5mg
0.25mg
12.5 mg
q.s |
54 |
Ambroxol Hcl, Levosalbutamol & Guaiphenesin Syrup |
Each 5ml Contains :
Ambroxol Hydrochloride
Levosalbutamol Sulphate
Equ. to Levosalbutamol
Guaiphenesin
In a Flavoured SyrupyBase
Colour : Ponceau 4R |
IP
IP
IP |
15mg
0.5mg
50mg
q.s |
55 |
Ambroxol HCL, Terbutaline Sulphate, Guaiphenesin & Menthol Syrup |
Each 5ml contains:
Ambroxol HCL
Terbutaline Sulphate
Guaiphenesin
Menthol
In a flavoured sugar free base |
IP
IP
IP
IP |
15mg
1.25mg
50mg
1mg
q.s. |
56 |
Ambroxol Hydrochloride , Phenylephrine Hydrochloride ,Chlorpheniramine Maleate, Guaiphenesin & Menthol Syrup |
Each 5ml. contains :
Phenylephrine HCL
Ambroxol Hydrochloride
Guaiphenesin
Chlorpheniramine Maleate
Menthol
In a Flavoured syrupybase
Approved colour used. |
IP
IP
IP
IP
IP |
5mg
15mg
50mg
2mg
1.5mg
q.s. |
57 |
Ambroxol Hydrochloride (SR)& Levocetirizine hydrochloride Tablets |
Each Filmcoated Tablet Contains:-
Ambroxol Hydrochloride
(As sustained Release)
Levocetirizinehydrochloride
Excipients
Approved colour used |
P
IP |
75 mg
5mg
q.s. |
58 |
Ambroxol Hydrochloride & Cetirizine Hydrochloride Syrup |
Each 5ml contains :
Ambroxol Hydrochloride
Cetirizine Hydrochloride
In a Flavoured SyrupyBase.
Approved colour used |
IP
IP |
30mg
5mg
q.s. |
59 |
Ambroxol Hydrochloride Syrup |
Each 5ml contains :
Ambroxol Hydrochloride
In a Flavoured SyrupyBase
Approved colour used |
IP |
30mg
q.s. |
60 |
Ambroxol Hydrochloride Terbutaline Sulphate, Guaiphenesin & Menthol Syrup |
Each 5ml. contains :
Ambroxol Hydrochloride
Terbutaline Sulphate
Guaiphenesin
Menthol
In a Sorbitol Solution (70%)
(Non-Crystallising)
Approved colour used |
IP
IP
IP
IP |
15mg
1.25mg
50mg
2.5mg
q.s. |
61 |
Ambroxol Hydrochloride, Levosalbutamol Sulphate & Guaiphenesin Syrup |
Each 5ml Contains
Ambroxol Hydrochloride
Levosalbutamol Sulphate
Eq. to Levosalbutamol
Guaiphenesin
In flavoured Syrupybase
Approved colour used |
IP
IP
IP |
30 mg
1 mg
50mg
q.s. |
62 |
Ambroxol Hydrochloride, Terbutaline Sulphate & Guaiphenesin oral Drops |
Each ml(Approx. 20drops) contains :
Ambroxol Hydrochloride
Terbutaline Sulphate
Guaiphenesin
In a flavoured syrupyBase.
Approved colour used. |
IP
IP
IP |
7.5mg
0.5mg
12.5mg
q.s. |
63 |
Ambroxol Terbutaline Guaiphenesin with Menthol Syrup |
Each 5ml Contains :-
Ambroxol Hydrochloride
Terbutaline Sulphate
Guaiphenesin
Menthol
In flavoured syrupyBase
Approved Colour Used. |
IP
IP
IP
IP |
15mg
1.25mg
50mg
2.5mg
q.s. |
64 |
Ambroxol Terbutaline Guaiphenesin with Menthol Syrup |
Each 5ml Contains :-
Ambroxol Hydrochloride
Terbutaline Sulphate
Guaiphenesin
Menthol
In flavoured syrupyBase
Approved Colour Used. |
IP
IP
IP
IP |
30mg
2.5mg
100mg
2.5mg
q.s. |
65 |
Amisulpride Tablets IP |
Each Uncoated Tablet Contains:
Amisulpride
Excipients
Approved colour used. |
IP |
100mg
q.s. |
66 |
Amitriptyline Hydrochloride Tablets IP |
Each film coated tablet contains:-
Amitriptyline Hydrochloride
Excipients
Colour:- Approved Colour used |
IP |
10 mg
q.s |
67 |
Amitriptyline Hydrochloride Tablets IP |
Each film coated tablet contains:-
Amitriptyline Hydrochloride
Excipients
Colour:- Approved Colour used |
IP |
25 mg
q.s. |
68 |
Amitriptyline Hydrochloride Tablets IP |
Each film coated tablet contains:-
Amitriptyline Hydrochloride
Excipients
Colour:- Approved Colour used |
IP |
50 mg
q.s. |
69 |
Amlodipine & AtenololTablets |
Each uncoated tablet contains:-
Amlodipine Besylate
Equivalent to Amlodipine
Atenolol
Excipients
Colour:-Approved colour used |
IP
IP |
5 mg
50 mg
q.s. |
70 |
Amlodipine Tablets IP |
Each uncoated tablet contains:-
Amlodipine Besylate
Equivalent to Amlodipine
Excipients
Colour : Approved Coloured Used |
IP |
5 mg
q.s |
71 |
AmlodipineTablets IP |
Each uncoated Tablet contains:
Amlodipine Besylate
Equ. to Amlodipine
Excipients
Approved colour used |
IP |
2.5mg
q.s. |
72 |
AmlodipineTablets IP |
Each uncoated tablet contains:-
Amlodipine Besylate
Equivalent to Amlodipine
Excipients
Colour : Approved Coloured Used |
IP |
10 mg
q.s |
73 |
Amorolfine Cream 0.25% w/w |
Composition :
Amorolfine Hydrochloride
Equ. to Amorolfine
Excipients
Cream Base |
IP |
0.25%w/w
q.s. |
74 |
Artemether & Lumifantrine Tablets |
Each uncoatedTabletsContains:
Artemether
Lumifantrine
Excipients
Approved colour used |
IP |
80 mg
480 mg
q.s. |
75 |
Ascorbic Acid (Vitamin C ), Sodium Ascorbate & Zinc Chewable Tablets |
Each uncoated Tablet Contains:
Ascorbic Acid
Sodium Ascorbate
Equ. to Ascorbicacid
Zinc
Excipients
Approved Colour Used |
IP
IP |
100mg
450mg
400mg
5mg
q.s |
76 |
Ascorbicacid Tablet IP |
Each Uncoated ChewableTablet Contains
Ascorbic acid
Excipients
Colour : ApprovedColour Used |
IP |
500mg |
77 |
Atenolol Tablets IP |
Each Uncoated Tablet Contains:
Atenolol
Excipients
Colour : Approved Coloured Used |
IP |
50mg
q.s |
78 |
Atenolol Tablets IP |
Each Uncoated Tablet Contains:
Atenolol
Excipients
Colour : Approved Coloured Used |
IP |
100mg
q.s |
79 |
Atorvastatin & FinofibrateTablets |
Each filmcoated tablet contain
Atorvastin Calcium
Eq.to Atorvastin
Finofibrate
Excipients
Approved colour used |
IP
IP |
10 mg
160 mg
q.s. |
80 |
Atorvastatin and Aspirin Capsules |
Each hard gelatin capsule contains:
Atorvastatin Calcium
Equ. to Atorvastatin
(In IRPellets form)
Aspirin
(As enteric coated pellets)
Excipients
Approved Colour used in emptycapsules shells. |
IP
IP |
10mg
75mg |
81 |
Atorvastatin Tablets IP |
Each film coated tablet contains:-
Atorvastatin Calcium
Eq. toAtorvastatin
Excipients
Colour:-Approved colour used |
IP |
10 mg
q.s. |
82 |
Atorvastatin Tablets IP |
Each film coated tablet contains:-
Atorvastatin Calcium
Eq. toAtorvastatin
Excipients
Colour:-Approved colour used |
IP |
20 mg
q.s. |
83 |
Atorvastatin Tablets IP |
Each film coated tablet contains:-
Atorvastatin Calcium
Eq. toAtorvastatin
Excipients
Colour:-Approved colour used |
IP |
40 mg
q.s. |
84 |
Atorvastatin Tablets IP |
Each film coated tablet contains:-
Atorvastatin Calcium
Eq. toAtorvastatin
Excipients
Colour:-Approved colour used |
IP |
80 mg
q.s. |
85 |
Atorvastatin, Clopidogrel and Aspirin Capsules |
Each hard gelatin capsule contains:
Atorvastatin Calcium
Equ. to Atorvastatin
(as Pellets)
Clopidogrel Bisulphate
Equ. to Clopidogrel
( as Pellets)
Aspirin
(As enteric coated pellets)
Excipients
Approved Colour used in emptycapsules shells. |
IP
IP
IP |
20mg
75mg
75mg |
86 |
Azathioprine Tablets IP |
Each uncoated tablet contains:
Azathioprine
Excipients
Approved colour used. |
IP |
50mg
q.s. |
87 |
Azithromycin & Lacticacid Bacillus Tablet |
Each film coated tablet contains:
Azithromycin Dihydrate
Equ. toAzithromycin Anhydrous
Lactic acid Bacillus
Excipients
Approved colour used |
IP |
250mg
60 million
spores
q.s |
88 |
Azithromycin & Lacticacid Bacillus Tablet |
Each film coated tablet contains:
Azithromycin Dihydrate
Equ. toAzithromycin Anhydrous
Lactic acid Bacillus
Excipients
Approved colour used |
IP |
500mg
60 million
spores
q.s |
89 |
Azithromycin Dispersible Tablet |
Each uncoated dispersible Tablet Contains :
Azithromycin Dihydrate
Equ. to Azithromycin anhydrous
Excipients
Colour : Approved Coloured Used |
IP |
100mg |
90 |
Azithromycin Oral Suspension IP |
Each 5 ml contains
Azithromycin Dihydrate
eq. toAnhydrousAzithromycin
In a flavoured Syrupybase.
Approved Colour Used |
IP |
200mg
q.s. |
91 |
Azithromycin Suspension IP |
Each 5 ml contain:
Azithromycin Dihydrate
Equivalent to Azithromycin Anhydrous
In flavoured Syrupybase
Approved colour used |
IP |
100 mg
q.s |
92 |
Azithromycin Tablet IP |
Each film coated tablet contains:
Azithromycin Dihydrate
Equivalent to Azithromycin anhydrous
Excipients
Approved colour used |
IP |
250 mg
q.s. |
93 |
Azithromycin Tablet IP |
Each film coated tablet contains:
Azithromycin Dihydrate
Equivalent to Azithromycin anhydrous
Excipients
Approved colour used |
IP |
500 mg
q.s. |
94 |
B –Complex Capsules |
Each hard gelatin capsule contains
Vitamin B1 (Thiamine Mononitrate)
Vitamin B2 (Riboflavin)
Vitamin B6 (Pyridoxine Hydrochloride) Niacin
(Nicotinamide)
Pantothenic Acid (Calcium D-Pantothenate) Vitamin B12
(Cyanocobalamin)
Folic Acid (n-pteroyl L-Glutamic Acid)
Zinc (as Zinc Sulphate)
Bacillus Coagulans
Biotin (D-Biotin)
Excipients
Approved colour used in emptycapsule shells. |
IP
IP
IP
IP
IP
IP
IP
IP
IP |
1.1mg
1.3mg
2mg
14mg
5mg
1mcg
100mcg
10mg
2000 Millions
30mcg
q.s |
95 |
B- Complex Capsules |
Each hard gelatin capsule contains
Thiamine Mononitrate
Riboflavin Sodium Phosphate
Pyridoxine Hydrochloride
Niacinamide
Calcium Pantothenate
Vitamin B12
Folic Acid
Biotin
Ascorbicacid
Excipients
Approved colour used in emptycapsule shells. |
IP
IP
IP
IP
IP
IP
IP
USP
IP |
10mg
10mg
3mg
100mg
50mg
15mcg
1.5 mg
100mcg
150mg
q.s |
96 |
B-complex with L- Lysine Capsules |
Each hard gelatin capsule contains
Thiamine Mononitrate
Riboflavin Sodium Phosphate
Pyridoxine Hydrochloride
Niacinamide
Calcium Pantothenate
Vitamin B12
Folic Acid
L-Lysine Mono Hydrochloride
Excipients
Approved colour used in emptycapsule shells. |
IP
IP
IP
IP
IP
IP
IP
USP |
10mg
10mg
3mg
50mg
20mg
5mcg
1000mcg
150mg
q.s |
97 |
B-Complex with L- Lysine Syrup |
Each 5ml contains :
L-Lysine Monohydrochloride
Vitamin B1
Vitamin B2
Vitamin B6
Methylcobalamin
Niacinamide
Zinc Sulphate
Ina pleasantlySyrupyBase
Colour : Tartrazine FCF |
USP
IP
IP
IP
IP
IP
IP |
25mg
1.5mg
1.0mg
0.5mg
2mcg
15mg
2.0mg
q.s |
98 |
B-Complex with Lysine Syrup |
Each 5ml contains :-
Lysine Hydrochloride
Pyridoxinehydrochloride
Niacinamide
Cyanocobalamin
D- Panthenol
Zinc SulphateMonohydrate
Equ. toElemental zinc
In flavored syrupybase
ApprovedColour Used |
USP
IP
IP
IP
IP
IP |
200mg
1.5mg
25mg
7.5mcg
5mg
16.5mg
q.s. |
99 |
Baclofen Tablets IP |
Each uncoated tablet contains:
Baclofen
Excipients
Approved colour used. |
IP |
10mg
q.s. |
100 |
Baclofen Tablets IP |
Each uncoated tablet contains:-
Baclofen
Excipients
Approved colour used. |
IP |
25mg
q.s |
101 |
Baclomethasone Dipropionate, Neomycin and Clotrimazole Cream |
Composition
Baclomethasone Dipropionate
Neomycin sulphate
Clotrimazole
In cream base |
strength |
0.025 %w/w
0.5 % w/w
1 % w/w
q.s. |
102 |
Beclomethasone Dipropionate, Phenylephrine Hydrochloride & Lignocaine Hydrochloride Cream |
Composition:
Beclomethasone Dipropionate
Phenylephrine Hydrochloride
Lignocaine Hydrochloride
Preservative Chlorocresole
Aqueous cream base |
IP
IP
IP
IP |
0.025%w/w
0.10% w/w
2.50% w/w
0.1% w/w
q.s. |
103 |
Benfotiamine Mecobalamin , Alpha Lipoic acid, Inositol , Pyridoxine Hydrochloride & Folicacid Capsules |
Each hard gelatin capsule contains
Benfotiamine
Mecobalamin
Alpha Lipoic acid ,
Inositol ,
Pyridoxine Hydrochloride
Folic acid
Excipients
Approved colour used in emptycapsule shells. |
IP
IP
USP
IP
IP
IP |
100mg
1000mcg
200mg
100mg
3mg
1.5mg
q.s |
104 |
Betahistine Tablet (SR) IP |
Each uncoated sustainedrelease tablet contain:
Betahistine Hydrochloride
Excipients
Approved colour used |
IP |
24 mg
q.s. |
105 |
Betahistine Tablet IP |
Each Uncoated Tablet Contains:-
Betahistine hydrochloride
Excipients
Approved colour used |
IP |
8mg
q.s |
106 |
Betahistine Tablet IP |
Each Uncoated Tablet Contains:-
Betahistine hydrochloride
Excipients
Approved colour used |
IP |
16 mg
q.s. |
107 |
Betahistine Tablets IP |
Each uncoated Tablet contains:
Betahistine Hydrochloride
Excipients
Approved colour used. |
IP |
24mg
q.s. |
108 |
Betahistine Tablets IP |
Each uncoated tablets contains:
Betahistine Hydrochloride
Excipients
Approved colour used |
IP |
8 mg
q.s. |
109 |
Betahistine Tablets IP |
Each uncoated tablets contains:
Betahistine Hydrochloride
Excipients
Approved colour used |
IP |
16 mg
q.s. |
110 |
Betamethasone Tablets IP |
Each uncoated tablet contains:-
Betamethasone
Excipients
Colour : Approved Coloured Used |
IP |
0.5mg
q.s. |
111 |
Bilastine & Montelukast Tablets |
Each Film Coated bilayered tablet Contains:
Montelukast Sodium eq. to
Montelukast
Bilastine
Excipients
Approved colour used. |
IP |
10mg
20mg
q.s. |
112 |
Bilastine Tablets |
Each Film Coated Tablet Contains:
Bilastine
Excipients
Approved colour used |
|
20mg
q.s. |
113 |
Biotin & FolicAcid Tablets |
Each film coated Tablet contains:
Biotin
Folic Acid
Excipients
Approved Colour used |
USP
IP |
5mg
5mg
q.s |
114 |
Biotin Tablets USP |
Each Film coated Tablet Contains :
Biotin
Excipients
Approved colour used |
USP |
10mg
q.s. |
115 |
Bisacodyl Tablets IP |
Each enteric coated tablet contains:
Bisacodyl
Excipients
Approved colour used |
IP |
5mg
q.s. |
116 |
Bisoprolol Fumarate Tablets |
Each film coated tablet contains:
Bisoprolol Fumarate
Excipients
Approved colour used. |
IP |
2.5mg
q.s. |
117 |
Bisoprolol Fumerate Tablets |
Each film coated tablet contains:
Bisoprolol Fumerate
Excipients
Approved colour used. |
IP |
5mg
q.s. |
118 |
Bromhexine Hydrochloride, Terbutaline Sulphate, Guaiphenesin &Menthol Syrup |
Each 5ml contains :
Bromhexine Hydrochloride
Terbutaline Sulphate
Guaiphenesin
Menthol
In a flavoured SyrupyBase.
Approved colour used. |
IP
IP
IP
IP |
4mg
1.25mg
50mg
2.5mg
q.s |
119 |
Calamine & Liquid Paraffin Lotion |
Composition :
Calamine
Liquid Paraffin
Lotion Base |
IP
IP |
8.0%w/w
10%w/w
q.s. |
120 |
Calcitriol & Calcium Citrate Suspension |
Each 5ml contains:
Calcitriol
Calcium Citrate
Equ. To Elemental
CalciumIn a Flavoured
syrupyBase.Approved
colour used. |
IP
USP |
0.0625mcg
100mg
q.s. |
121 |
Calcium Carbonate & Vitamin D3 Tablets |
Each film coated Tablet contains:
Calcium Carbonate
(Derived from an organic source oyster shell)
Equ. to Elemental Calcium
Vitamin D3
Excipients
Approved colour used |
IP
IP |
1250mg
500mg
500IU
q.s. |
122 |
Calcium Carbonate, & Vitamin D3 Suspension |
Each 5ml Contains :
Calcium Carbonate 625mg
(Derived from Oyster Shell)
Equ. to elemental Calcium
Vitamin D3
Flavoured SyrupyBase
ApprovedColour Used |
IP
IP |
250mg
125IU
q.s. |
123 |
Calcium Carbonate, Magnesium Hydroxide, Zinc & Vitamin D3 Suspension |
Each 5ml contains:
Calcium Carbonate
Eq. toElementalCalcium
Magnesium Hydroxide
Eq. toElemental Magnesium
Zinc Gluconate
Eq. toElemental zinc
Vitamin D3
In a Flavoured syrupybase
Approved colour used |
IP
IP
USP
IP |
625 mg
250 mg
180 mg
75 mg
14 mg
2 mg
200 IU |
124 |
Calcium Carbonate, Vitamin d3 Magnesium& Zinc Suspension. |
Each 5ml contains:
Calciumcarbonate
(eq. toElemental calcium150mg)
Vitamin D3
Magnesium Hydroxide
(Eq.to Elemental magnesium)
Zinc Gluconate
Eq.to Elemental zinc
In flavored syrupybase
ApprovedColour Used |
IP
IP
IP
IP |
375mg
200IU
25mg
10.45mg
1.5mg
q.s. |
125 |
Calcium Carbonate, Vitamin D3, Methylcobalamin, L-Methylfolate Calcium & Pyridoxal-5- Phosphate Tablets |
Each Film Coated Tablet Contains :
Calcium Carbonate( from Oyster shell)
Equ. to Elemental Calcium
Vitamin D3
Methylcobalamin
L- Methylfolate Calcium
Pyridoxal-5- Phosphate
Excipients
Approved colour used. |
IP
IP |
1250mg
500mg
2000IU
1500mcg
1mg
20mg
q.s. |
126 |
Calcium Citrate Maleate, Calcitriol , Folic Acid , Zinc & Vitamin K2-7 Tablets |
Each Film Coated Tablet Contains:
Calcium Citrate Maleate
Equ. toElemental Calcium
Calcitriol
Folic Acid
Zinc Sulphate Monohydrate
Equ. to Zinc
Vitamin K2-7
Excipients
Approved colour used |
IP
IP
IP |
250mg
0.25mcg
100mcg
7.5mg
50mcg
q.s. |
127 |
Calcium Citrate Maleate, Methylcobalamin, Vitamin D3, Vitamin K2-7, Magnesium Oxide & Zinc Oxide Tablets |
Each film coated tablet contains:
Calcium Citrate Maleate
Methylcobalamin
Vitamin D3
Vitamin k2-7
Zinc Oxide
Magnesium Oxide
Excipients
Approved colour used |
IP
IP
IP
IP |
1250mg
1500mcg
1000IU
90mcg
15mg
50mg
q.s. |
128 |
Calcium Citrate Maleate& Vitamin D3 Tablets |
Each film coated Tablet Contains:
Calcium Citrate Maleate
Equ.ToElemental
CalciumVitamin D3
Excipients
Approved colour used |
USP
IP |
1250mg
250mg
450IU
q.s. |
129 |
Calcium Citrate, Calcitriol , Zinc & Manganese Tablets |
Each film coated tablet contains:
Calcium Citrate
Calcitriol
Zinc Sulphate Monohydrate
Eq. to elemental Zinc
Manganese (as Manganese Sulphate)
Excipients
Approved colour used. |
USP
BP
IP
IP |
1000 mg
0.25 mcg
7.5 mg
40 mg
q.s. |
130 |
Calcium Citrate, Magnesium, Zinc With Vitamin D3 Tablets |
Each film coatedTablet Contains:
Calcium Citrate
Magnesium Hydroxide
Zinc SulphateMonohydrate
Equ. to Elemental Zinc
Vitamin D3
Excipients
Approved Colour Used. |
USP
IP
IP
IP |
1000mg
100mg
4mg
200IU
q.s. |
131 |
Calcium Orotate & Vitamin D3 Tablets |
Each film coated tablet contains:
Calcium Orotate
Vitamin D3 (Stabilized)
Excipients
Approved colour used.
Appropriate overages of vitamin added to compensate the
loss on storage. |
I.P. |
740mg
1000 IU
q.s. |
132 |
Calcium Pantothenate Tablets I.P. 200mg |
Each film coated tablet contains:
D-Calcium Pantothenate
Excipients
Approved colour used. |
I.P. |
200mg
q.s. |
133 |
Calcium Phosphorus, Magnesium, Zinc& Vitamin D3 Suspension |
Each 10ml (2Teaspoonful) Contains:
Calcium Phosphate
Equ. To Elemental Calcium
Equ. ToElemental
PhosphorusMagnesium
Hydroxide
Equ. ToElemental
MagnesiumZinc Gluconate
Equ. ToElemental
ZincVitamin D3
In a Flavoured Palatable Base
Approved colour used. |
IP
IP
USP
IP |
300mg
150mg
75mg
4mg
400IU
q.s. |
134 |
Calcium, Vitamin D3, Vitamin B12 & Lysine Hydrochloride Suspension |
Each 5ml contains:
Calciumcarbonate
Equ. toElemental Calcium
Vitamin D3
Vitamin B12
Lysine Hydrochloride
Flavoured sorbitol base.
Approved colour used. |
IP
IP
IP
USP |
150mg
200IU
2.5mcg
25mg
q.s. |
135 |
Calcium,Vitamin D3, Methylcobalamin, L-Methylfolate Calcium & Pyridoxal-5- Phosphate Tablets |
Each film coated tablet contains:
Calcium Carbonate
eq.to Elemental Calcium
Vitamin D3
Mecobalamin
(Methylcobalamin)
L-Methylfolate calcium
Pyridoxal-5-Phosphate
Excipients
Approved colour used. |
IP
IP
IP |
1250mg
500mg
2000 I.U.
1500mcg
1mg
20mg
q.s. |
136 |
Calcium&Vitamin D3 Tablets IP |
Each Film coated Tablet Contains:
Calcium Carbonate
Equ.toElemental Calcium
Vitamin D3
Excipients
Approved Colour Used. |
IP
IP |
500mg
250IU
q.s. |
137 |
Carbamazepine Tablets IP |
Each uncoated tablet contains:-
Carbamazepine
Excipients
Colour:- Approved Colour used |
IP |
200 mg
q.s. |
138 |
Carbimazole Tablets IP |
Each Film coated Tablet Contains :
Carbimazole
Excipients
Approved colour used |
IP |
5mg
q.s. |
139 |
Carbonyl Iron, folic acid, Vitamin B12 and Zinc Sulphate Capsules |
Each hardgelatin capsule contain:
Carbonyl Iron
Equivalent toElemental Iron
Folic acid
Vitamin B12
Zinc sulphate monohydrate
Equivalent to elemental zinc
Excipients
Approved colour used in emptycapsule shells |
IP
IP
IP |
100 mg
1.5 mg
15mcg
22.5 mg
q .s. |
140 |
Carisoprodol Tablets IP |
Each Uncoated tablet contains:-
Carisoprodol
Excipients
Colour:- Approved Colour used |
IP |
350 mg
q.s |
141 |
Carvedilol Tablets IP |
Each Uncoated Tablet contains:
Carvedilol
Excipients
Approved colour used |
IP |
3.125mg
q.s. |
142 |
Carvedilol Tablets IP |
Each uncoated Tablet Contains:
Carvedilol
Excipients
Approved colour used |
IP |
12.5mg
q.s. |
143 |
Carvedilol Tablets IP |
Each Uncoated Tablet contains:
Carvedilol
Excipients
Approved colour used |
IP |
6.25mg
q.s. |
144 |
Carvedilol Tablets IP |
Each film coated Tablet contains:
Carvedilol
Excipients
Approved colour used |
IP |
3.125mg
q.s. |
145 |
Celecoxib Capsules |
Each hard gelatin capsules contains:
Celecoxib
Excipients
Approved colour used in emptycapsule shell. |
IP |
200mg
q.s. |
146 |
Cetirizine Dihydrochloride, Dextromethorphan Hydrobromide & Phenylephrine Hydrochloride Syrup |
Each 5ml contains :
Dextromethorphan Hydrobromide
Cetirizine Dihydrochloride
Phenylephrine Hydrochloride
In a flavoured SyrupyBase
Approved colour Used |
IP
IP
IP |
10mg
5mg
5mg
q.s. |
147 |
Cetirizine HCl, Phenylephrine HCl & Paracetamol Tablets |
Each film coated tablet contains:
Cetirizine HCl
Phenylephrine HCl
Paracetamol
Excipients
Approved colour used.
(Banned drug 12/08/2024) |
IP
IP
IP |
5mg
5mg
325mg
q.s. |
148 |
Cetirizine Hydrochloride & Ambroxol Hydrochloride Tablets |
Each film coated tablet contains:
Cetirizine Hydrochloride
Ambroxol Hydrochloride
Excipients
Approved colour used. |
I.P.
I.P. |
5mg
60mg
q.s. |
149 |
Cetirizine Hydrochloride Syrup IP |
Each 5 ml contains:
Cetirizine Hydrochloride
In a flavoured syrupybase
Approved colour base |
IP |
5 mg
q.s. |
150 |
Cetirizine Hydrochloride Tablets IP |
Each uncoated tablet contains:-
Cetirizine Hydrochloride
Excipients
Colour:- Approved Colour used |
IP |
10 mg
q.s. |
151 |
Chlordiazepoxide & Clidinium Bromide Tablet |
Each FilmCoated tablet contains
Chlordiazepoxide
Clidinium Bromide
Excipients
Approved Colour used |
IP
IP |
5mg
2.5mg
q.s |
152 |
Chlorhexidine Gluconate, Metronidazole & Lignocaine Hydrochloride Gel |
Composition :-
Chlorhexidine Gluconate Solution
Equ. to Chlorhexidine
Metronidazole
Equ. to Metronidazole
Lignocaine Hydrochloride
Gel Base |
IP
IP
IP |
1%w/w
1%w/w
2%w/w
q.s. |
153 |
Chlorhexidine Gluconate, Sodium Fluoride & Zinc Chloride Mouthwash |
Composition :
Chlorhexidine Gluconate
(as Chlorhexidine Gluconate Solution IP)
Sodium Fluoride
ZincChloride
Base
Colour: Brilliant Blue FCF |
IP
IP |
0.2%w/v
0.05%w/v
0.09%w/v
q.s |
154 |
Chlorhexidine GluconateSolution & Cetrimide Antiseptic Liquid |
Composition:
ChlorhexidineGluconate solution
Cetrimide
Solution Base |
IP
IP |
0.3% v/v
0.6% w/v
q.s. |
155 |
Chlorhexidine mouth wash IP |
Chlorhexidine Gluconate Solution
diluted to Chlorhexidine Gluconate
In a flavoured Aqueous base
Approved colour used. |
IP |
0.2% w/v
q.s. |
156 |
Chlorpheniramine Maleate tablet IP |
Each Uncoated Tablet Contains:
Chlorpheniramine Maleate
Equ. to Chlorpheniramine
Excipients |
IP |
4mg
q.s. |
157 |
Chlorpheniramine Maleate, Phenylephrine Hydrochloride & Dextromethorphan Hydrobromide Syrup |
Each 5ml contains :
Chlorpheniramine Maleate
Phenylephrine Hydrochloride
Dextromethorphan Hydrobromide
In a flavoured palatable base
Approved colour used. |
IP
IP
IP |
2mg
5mg
15mg
q.s. |
158 |
Chlorpromazine Hydrochloride Tablets IP |
Each film coated tablet contains:-
Chlorpromazine Hydrochloride
Excipients
Colour:- Approved Colour used |
IP |
50 mg
q.s. |
159 |
Chlorpromazine Hydrochloride Tablets IP |
Each film coated tablet contains:-
Chlorpromazine Hydrochloride
Excipients
Colour:- Approved Colour used |
IP |
100 mg
q.s. |
160 |
Chlorpromazine Hydrochloride Tablets IP |
Each film coated Tablet Contains:
Chlorpromazine Hydrochloride
Excipients
Approved colour used. |
IP |
50mg
q.s. |
161 |
Chlorzoxazone, Diclofenac Potassium, Paracetamol |
Each film coated tablet contains:
Chlorzoxazone
Diclofenac Potassium
Paracetamol
Excipients
Approved colour used. |
USP
BP
IP |
250mg
50mg
325mg
q.s. |
162 |
Cholecalciferol GranulesSachet |
Each sachet of1gmContains:
Cholecalciferol
Excipients |
IP |
60000 IU
q.s |
163 |
Cholecalciferol oral solution USP |
Each ml Contains:
Cholecalciferol
(Vitamin D3)
In a pleasantlyflavoured palatable Base
Approved Colour used. |
IP |
400IU
q.s. |
164 |
Cholecalciferol Tablet IP |
Each uncoated chewable tablet contains
Cholecalciferol (Stabilized)
Excipients
Colour :- Approved colour used |
IP |
60000IU
q.s. |
165 |
Cholecalciferol, Ferrous Ascorbate, Folic Acid & Cyanocobalamin Tablets |
Each film coated Tablet Contains:
Cholecalciferol
Ferrous Ascorbate
Equ. toElemental Iron
Folic Acid
Cyanocobalamin
Excipients
Approved colour used |
IP
IP
IP |
1000IU
100mg
1mg
7.5mcg
q.s. |
166 |
Choline Salicylate & Lignocaine Hydrochloride Gel |
Composition :
Choline Salicylate Solution
Equ. to Choline Salicylate
Lignocaine Hydrochloride
Preservative:
Benzalkonium Chloride
In Pleasant Flavoured Base |
BP
IP
IP |
8.7%w/w
2.0%w/w
0.01%w/w
q.s |
167 |
Choline Salicylate, Lignocaine Hydrochloride and Benzalkonium Chloride Gel |
Composition :
Choline Salicylate Solution
Equ. to Choline Salicylate
Lignocaine Hydrochloride
Benzalkonium Chloride
In a Flavoured Mucoadhesive gel base |
BP
IP
IP |
8.7%w/w
2.0%w/w
0.01%w/w
q.s |
168 |
Cilnidipine Tablet |
Each film coated tablet contains
Cilnidipine
Excipients
Colour :- Approved Colour Use |
IP |
10mg
q.s |
169 |
Cilnidipine Tablets IP |
Each film coated tablet contains:
Cilnidipine
Excipients
Approved colour used. |
IP |
5mg
q.s. |
170 |
Cilnidipine Tablets IP |
Each film coated tablet contains:
Cilnidipine
Excipients
Approved colour used. |
IP |
5mg
q.s. |
171 |
CilnidipineTablets IP |
Each film coated Tablet contains:
Cilnidipine
Excipients
Approved colour used. |
IP |
20mg
q.s. |
172 |
Cilostazol Tablets IP |
Each uncoated tablet contains:
Cilostazol
Excipients
Approved colour used. |
IP |
50mg
q.s. |
173 |
Cilostazol Tablets IP |
Each uncoated tablet contains:
Cilostazol
Excipients
Approved colour used. |
IP |
100mg
q.s. |
174 |
Cinnarizine (SR)Tablet IP |
Each uncoatedtablet contain:
Cinnarizine
(AsSustained Release)
Excipients
Approved colour used |
IP |
75 mg
q.s. |
175 |
Cinnarizine and Dimenhydrinate Tablets |
Each uncoated Tablet contains:
Cinnarizine
Dimenhydrinate
Excipients
Approved Colour used |
IP
BP |
20mg
40mg
q.s |
176 |
Cinnarizine Tablet IP |
Each uncoated tablet contain:
Cinnarizine
Excipients
Approved colour used |
IP |
25 mg
q.s. |
177 |
Cinnarizine Tablets IP |
Each uncoated Tablet contains
Cinnarizine
Excipients
Approved Coloured used |
IP |
75mg
q.s |
178 |
Cinnarizineand Domperidone Tablets |
Each uncoatedTabletsContains:
Cinnarizine
Domperidone
Excipients
Approved colour used |
IP
IP |
20 mg
15 mg
q.s. |
179 |
Ciprofloxacin and Tinidazole Tablets |
Each film coated Tablet contains:
Ciprofloxacin Hydrochloride
Equ. to Ciprofloxacin
Tinidazole
Excipients
Approved colour used |
IP
IP |
250mg
300mg
q.s |
180 |
Ciprofloxacin HCl, Fluocinolone Acetonide , Clotrimazole & Chlorocresol Cream |
Composition :
Ciprofloxacin Hydrochloride
Equ. to Ciprofloxacin
Fluocinolone Acetonide
Clotrimazole
Chlorocresol
( as preservative)
Cream Base |
IP
IP
IP
IP |
0.5%w/w
0.01%w/w
1.0% w/w
0.1%w/w
q.s. |
181 |
Ciprofloxacin Tablets IP |
Each film coated tablet contains:-
Ciprofloxacin Hydrochloride
Eq. tociprofloxacin
Excipients
Colour:-Approved colour used |
IP |
250 mg
q.s. |
182 |
Ciprofloxacin Tablets IP |
Each film coated tablet contains:-
Ciprofloxacin Hydrochloride
Eq. tociprofloxacin
Excipients
Colour:-Approved colour used |
IP |
500 mg
q.s. |
183 |
Ciprofloxacin, Metronidazole, Terbinafine Hydrochloride & Clobetasol PropionateCream |
Composition :
Ciprofloxacin Hydrochloride
equ. to Ciprofloxacin
Metronidazole Benzoate
equ. to Metronidazole
Terbinafine Hydrochloride
Clobetasol Propionate
Preservatives :
Methyl Paraben
Propyl Paraben
Cream Base |
IP
IP
IP
IP
IP
IP |
1.0%w/w
1.0%w/w
1.0%w/w
0.05%w/w
0.16%w/w
0.033%w/w
q.s |
184 |
Citicoline & Piracetam Syrup |
Each 5ml contains:
Citicoline sodium
Equ. to Citicoline
Piracetam
Flavoured Syrupybase
Approved colour used |
IP
IP |
500mg
400mg
q.s |
185 |
Citicoline & PiracetamTablets |
Each FilmcoatedTabletsContains:
Piracetam
Citicoline sodium
Equivalent toCiticoline
Excipients
Approved colour used |
IP
IP |
800 mg
500 mg
q.s. |
186 |
CiticolineTablets |
Each FilmcoatedTabletsContains:
Citicoline sodium
Equivalent toCiticoline
Excipients
Approved colour used |
IP |
500 mg
q.s. |
187 |
Clarithromycin Tablet IP |
Each film coatedtablet contain:
Clarithromycin
Excipients
Approved colour used |
IP |
500 mg
q.s |
188 |
Clarithromycin Tablet IP |
Each film coated tablet Contains:-
Clarithromycin
Excipients
Colour :-Approved colour used |
IP |
250mg
q.s |
189 |
Clindamycin & NicotinamideGel |
Composition:
Clindamycin Phosphate
Equivalent toClindamycin
Nicotinamide
Gel base |
IP
IP |
1.0% w/w
4.0% w/w
q.s. |
190 |
Clindamycin Hydrochloride Capsule IP |
Each hardgelatin capsule contain:
Clindamycin Hydrochloride
Equivalent to Clindamycin
Excipients
Approved colour used in emptyhard gelatin capsule |
IP |
300 mg |
191 |
Clindamycin Phosphate & AdapaleneGel |
Composition
Clindamycin phosphate
Equivalent to clindamycin
Adapalene
Gel base |
IP
IP |
1 % w/w
0.1%w/w
q.s. |
192 |
Clindamycin PhosphateGel |
Composition:-
Clindamycin Phosphate
Equivalent toClindamycin
Benzoyl PeroxideAnhydrous
Gel Base |
IP
IP |
1.00% w/w
2.50% w/w |
193 |
Clobetasol Propionate , Miconazole Nitrate, Neomycin Sulphate Cream |
Composition :
Clobetasol Propionate
Miconazole Nitrate
Neomycin Sulphate
Equ.toNeomycin Base
Chlorocresol
(as preservative)
Cream base |
IP
IP
IP
IP |
0.05%w/w
2%w/w
0.5%w/w
0.1%w/w
q.s. |
194 |
Clobetasol Propionate & Salicylic Acid Ointment |
Composition:
Clobetasol Propionate
Salicylic acid
Excipients
In Ointment Base |
IP
IP |
0.05%w/w
6.0%w/w
q.s. |
195 |
Clobetasol Propionate &Fusidic Acid Cream |
Composition:
Clobetasol Propionate
Fusidic Acid
In a water Miscible Cream Base
Preservatives:
Butylated Hydroxytoluene
Sorbic Acid |
IP
IP
IP
IP |
0.05%W/W
2.00%W/W
0.005%W/W
0.200%W/W |
196 |
Clobetasol Propionate cream IP |
Composition:
Clobetasol Propionate
Cream Base |
IP |
0.05%w/w
q.s. |
197 |
Clobetasol Propionate, Fusidic Acid,Clotrima zole Cream |
Composition:
Clobetasol Propionate
Fusidic Acid
Clotrimazole |
USP
IP
IP |
0.05%W/W
2%W/W
1%W/W |
198 |
Clobetasol Propionate, Gentamicin, Tolnaftate, Iodochlorhydroxyq uinoline and Clotrimazole Cream |
Composition :
Clobetasol Propionate
Gentamicin Sulphate
Equ. to Gentamicin
Tolnaftate
Iodochlorhydroxyquinoline
Clotrimazole
Preservative :
Chlorocresol
Cream base |
IP
IP
IP
IP
IP
IP |
0.05%w/w
0.10%w/w
1.0%w/w
1.0%w/w
1.0%w/w
q.s. |
199 |
Clobetasol Propionate, Neomycin Sulphate, Tolnaftate, Iodochlorhydroxyq uinoline and Ketoconazole Cream |
Composition
Clobetasol Propionate
Neomycin Sulphate
Tolnaftate
Iodochlorhydroxyquinoline
Ketoconazole
In a Non greasycream base |
IP
IP
IP
IP
IP |
0.05% w/w
0.1% w/w
1.0% w/w
1.0% w/w
2.0% w/w
q.s |
200 |
Clobetasol Propionate, Ofloxacin, Itraconazole, Cream |
Composition :
Ofloxacin
Ornidazole
Itraconazole
Clobetasol
Propionate
Methylparaben(As preservative)
Propylparaben
( As preservative)
Cream Base |
IP
IP
USP
IP
IP
IP
IP |
0.75%w/w
2.0%w/w
1.00%w/w
0.05%w/w
0.20%w/w
0.02%w/w
q.s. |
201 |
Clobetasol, Neomycin & Clotrimazole Cream |
Composition :
Clobetasol Propionate
Neomycin Sulphate
Clotrimazole
Preservatives:
Chlorocresol
Cream Base |
IP
IP
IP
IP |
0.05%w/w
0.5%w/w
1.0%w/w
0.1%w/w
q.s. |
202 |
Clomifene Tablets IP |
Each uncoated tablet contains:
Clomifene Citrate
Excipients
Approved colour used. |
IP |
50mg
q.s. |
203 |
Clomiphene Citrate Tablets IP |
Each Uncoated Tablet Contains:
Clomiphene Citrate
Excipients |
IP |
50mg
q.s. |
204 |
Clomiphene Tablet IP |
Each uncoated Tablet Contains :-
Clomiphene Citrate
Excipients
Colour :- Approved colour used |
IP |
50mg
q.s |
205 |
Clonazepam Tablet IP |
Each uncoated Tablet contains:
Clonazepam
Excipients
Approved colour used |
IP |
0.25mg
q.s |
206 |
Clonazepam Tablet IP |
Each uncoated Tablet contains:
Clonazepam
Excipients
Approved colour used |
IP |
0.5mg
q.s |
207 |
Clopidogrel and Aspirin Capsules |
Each hard gelatin capsule contains:
Clopidogrel Bisulphate
Equ. toClopidogrel
( as Pellets)
Aspirin
(As enteric coated pellets)
Excipients
Approved Colour used in emptycapsules shells. |
IP
IP |
75mg
75mg |
208 |
Clopidogrel Bisulphate Tablet |
Each film coated Tablet Contains:
Clopidogrel Bisulphate
Equ. toClopidogrel
Excipients
Colour : Approved Coloured Used |
IP |
75mg
q.s |
209 |
Clotrimazole & Beclomethasone Dipropionate Cream |
Composition :
Clotrimazole
Beclomethasone Dipropionate
Preservatives:
Benzyl Alcohol
Methyl Paraben
Cream base |
IP
IP
IP
IP |
1.0%w/w
0.025%w/w
1.0%w/w
0.15%w/w
q.s |
210 |
Clotrimazole Cream IP 1%w/w |
Composition
Clotrimazole
Preservatives :
Benzyl Alcohal
Water Miscible Base |
IP
IP |
1%w/w
1%w/w
q.s. |
211 |
Clotrimazole DustingPowder |
Composition :
Each 100gm contains
Clotrimazole
Excipients |
IP |
1gm
q.s |
212 |
Combikit of Azithromycin Tablet IP, Fluconazole Tablet IP & Secnidazole Tablet IP |
Each Combikit Contain:
A) Azithromycin Tablet IP(1Tablet)
Each film coated tablet contain:
Azithromycin Dihydrate
Equivalent to Azithromycin anhydrous
Approved colour used
B) FluconazoleTablet IP (1Tablet)
Each uncoated tablet contain:
Fluconazole
Approved colour used
C) SecnidazoleTablet IP(2Tablet)
Each film coated tablet contain:
Secnidazole
Approved colour used |
IP
IP
IP |
1 gm
150 mg
1 gm |
213 |
Cyclosporine Capsules IP |
Each Hard Gelatin Capsule Contains :
Cyclosporine
Excipients
Approved colour used. EmptyCapsule Shells. |
IP |
250mg
q.s. |
214 |
Cyproheptadine Hydrochloride & Tricholine Citrate Drops |
Each ml contains :
Cyproheptadinehydrochloride
Equ. toanhydrous Cyproheptadine Hydrochloride
Tricholine Citrate
In a Flavoured palatable Base
Approved colour used |
IP |
1.5mg
55mg
q.s. |
215 |
Cyproheptadine Hydrochloride & Tricholine Citrate Syrup |
Each 5ml Contains:-
Cyproheptadine Hydrochloride
Tricholine Citrate (65%)
Sorbitol Solution (70%)
In flavoured Syrupy base
Approved colour used |
IP
IP |
2 mg
275 mg
q.s. |
216 |
Cyproheptadine Hydrochloride Tablet IP |
Each uncoated tablet contains : -
Cyproheptadine Hydrochloride
(as anhydrous)
Excipients
Colour : Approved Colour Used |
IP |
4mg
q.s |
217 |
Cyproheptadine Tablet IP |
Each uncoated tablet contains:
Cyproheptadine Hydrochloride (Anhydrous)
Excipients
Approved colour used |
IP |
4 mg |
218 |
Cyproheptadine, B- Complex & Zinc Syrup |
Each 5ml contains :
Cyproheptadine Hydrochloride
Vitamin B1
Vitamin B6
Vitamin B12
Niacinamide
D-Panthenol
ZincSulphate
Equ.ToElemental Zinc
In a Flavoured SyrupyBase
Approved colour used. |
IP
IP
IP
IP
IP
IP
IP |
2mg
1mg
1.5mg
1mcg
15mg
1.5mg
1.8mg
q.s. |
219 |
Dapagliflozin & Metformin HCl (ER) Tablets |
Each film coated Tablet Contains :
Dapagliflozin Propanedial Monohydrate
Equ. To Dapagliflozin
Metformin Hydrochloride
(as Extended Release)
Excipients
Approved colour used |
IP |
10mg
1000mg
q.s. |
220 |
Dapagliflozin 10mg & Metformin HCl (ER) 500mg Tablets |
Each film coated Tablet Contains :
Dapagliflozin Propanedial Monohydrate
Equ. to Dapagliflozin
Metformin Hydrochloride
(as Extended Release)
Excipients
Approved colour used |
IP |
10mg
500mg
q.s. |
221 |
Dapagliflozin Tablet |
Each film coated tablet contain:
Dapagliflozin propanediol monohydrate
Eq. to Dapagliflozin
Excipients
Approved colour used |
|
10 mg
q.s |
222 |
Dapagliflozin Tablets |
Each film coated tablet contain:
Dapagliflozin propanediol monohydrate
Eq. to Dapagliflozin
Excipients
Approved colour used |
|
5 mg
q.s |
223 |
Dapoxetine Tablets IP |
Each film coated tablet contains:
Dapoxetine Hydrochloride
Equ. to Dapoxetine
Excipients
Approved colour used |
IP |
30 mg
q.s |
224 |
Dapoxetine Tablets IP |
Each film coated tablet contains:
Dapoxetine Hydrochloride
Equ. to Dapoxetine
Excipients
Approved colour used |
IP |
60 mg
q.s |
225 |
Deflazacort Oral Suspension |
Each 5ml contain:
Deflazacort
In flavoured Syrupybase
Approved colour used |
|
6 mg
q.s. |
226 |
Deflazacort Tablets |
Each uncoated tablet contains:
Deflazacort
Excipients
Colour:- Approved colour used |
IP |
12 mg
q.s. |
227 |
Deflazacort Tablets |
Each Uncoated Tablet Contains:
Deflazacort
Excipients
Approved Colour used |
|
18mg
q.s |
228 |
DeflazacortTablet |
Each uncoated tablet contain:
Deflazacort
Excipients
Approved colour used |
|
30 mg
q.s. |
229 |
DeflazacortTablets |
Each uncoated tablet contains:-
Deflazacort
Excipients
Colour:-Approved colour used |
IP |
6 mg
q.s. |
230 |
Desloratadine Tablet |
Each film coated Tablet Contains:-
Desloratadine
Excipients
Approved colour used |
BP |
5 mg
q.s. |
231 |
Desloratadine, Ambroxol Hydrochloride, Guaiphenesin & Menthol Syrup |
Each 5ml contains:
Desloratadine
Ambroxol Hydrochloride
Guaiphenesin
Menthol
Flavoured syrupybase.
Approved colour used. |
BP
IP
IP
IP |
2.5mg
30mg
50mg
1mg
q.s. |
232 |
Dexamethasone Tablets IP |
Each uncoated tablet contains:-
Dexamethasone
Excipients
Colour : Approved Coloured Used |
IP |
0.5 mg
q.s. |
233 |
Dexketoprofen Tablet |
Each film coated Tablet Contains:
Dexketoprofen trometamol
Equ. to Dexketoprofen
Excipients
Colour : Approved Coloured Used |
|
25mg
q.s |
234 |
Dexlansoprazole Modified Release Capsule |
Each Hard Gelatin Capsule Contains:
Dexlansoprazole
(as modified release pellets)
Excipients
Approved colour used. |
IP |
30mg
q.s. |
235 |
Dexlansoprazole Modified Release Capsule |
Each Hard Gelatin Capsule Contains:
Dexlansoprazole
(as modified release pellets)
Excipients
Approved colour used. |
IP |
60mg
q.s. |
236 |
Dexlansoprazole Modified Release Capsule |
Each Hard Gelatin Capsules Contains:
Dexlansoprazole
(as Modified Release Pellets)
Approved colour used in Pellets & EmptyCapsule Shells. |
IP |
60mg |
237 |
Dexrabeprazole (Enteric Coated) & Domperidone (Sustained Release) Capsule |
Each hardgelatin capsule contains :
Dexrabeprazole Sodium
(as Enteric Coated Pellets)
Domperidone
(as Sustained Release Pellets)
Excipients
Approved colour used. |
IP |
10mg
30mg
q.s. |
238 |
Dextromethorphan HBR, Ambroxol HCL, Chlorpheniramine Maleate, Phenylephrine HCL & Menthol Syrup |
Each 5 ml contains:
Dextromethorphan Hydrobromide
Ambroxol Hydrochloride
Chlorpheniramine Maleate
Phenylephrine Hydrochloride
Menthol
Flavoured syrupy base
Approved colour used |
IP
IP
IP
IP
IP |
10 mg
15 mg
4 mg
5 mg
1 mg
q.s |
239 |
Dextromethorphan HBR, Ambroxol HCL, Chlorpheniramine Maleate, Phenylephrine HCL & Menthol Syrup |
Each 5 ml contains:
Dextromethorphan Hydrobromide
Ambroxol Hydrochloride
Chlorpheniramine Maleate
Phenylephrine Hydrochloride
Menthol
Flavoured syrupy base
Approved colour used |
IP
IP
IP
IP
IP |
10 mg
15 mg
2 mg
5 mg
1.5 mg
q.s |
240 |
Dextromethorphan HBR, Bromhexine HCL & Phenylephrine HCL Syrup |
Each 5 ml Contains:
Dextromethorphan Hydrobromide
Bromhexine Hydrochloride
Phenylephrine Hydrochloride
In a flavoured syrupybase
Approved colour base |
IP
IP
IP |
5 mg
4 mg
5 mg
q.s. |
241 |
Dextromethorphan HBR, Chlorpheniramine Maleate, Phenylephrine HCL Tablets |
Each uncoated tablet Contains:
Dextromethorphan Hydrobromide
Chlorpheniramine Maleate
Phenylephrine Hydrochloride
Excipients
Approved colour used |
IP
IP
IP |
10 mg
2 mg
5 mg
q.s. |
242 |
Dextromethorphan HBR, Phenylephrine HCL & Chlorpheniramine Maleate Syrup |
Each 5ml Contains:-
Dextromethorphan Hydrobromide
Phenylephrine Hydrochloride
Chlorpheniramine Maleate
In flavoured Syrupybase
Approved colour used |
IP
IP
IP |
10 mg
5 mg
2mg
q.s. |
243 |
Dextromethorphan Hydrobromide & Chlorpheniramine maleate Syrup |
Each 5 ml contains :-
Dextromethorphan Hydrobromide
Chlorpheniramine maleate
In flavoured syrupyBase
Approved Colour Used. |
IP
IP |
10mg
4mg
q.s. |
244 |
Dextromethorphan Hydrobromide & Chlorpheniramine maleate Syrup |
Each 5 ml contains :-
Dextromethorphan Hydrobromide
Chlorpheniramine maleate
In flavoured syrupyBase
Approved Colour Used. |
IP
IP |
10mg
2mg
q.s. |
245 |
Dextromethorphan Hydrobromide, Cetirizine Hydrochloride, Ammonium Chloride, Ambroxol Hydrochloride & Menthol Syrup |
Each 5ml contains :
Dextromethorphan Hydrobromide
Cetirizine Hydrochloride
Ammonium Chloride
Ambroxol Hydrochloride
Menthol
In a flavoured SyrupyBase
Approved colour used. |
IP
IP
IP
IP
IP |
10mg
2.5mg
100mg
30mg
1mg
q.s. |
246 |
Dextromethorphan Hydrobromide, Phenylephrine hydrochloride & Chlorpheniramine Maleate Tablets |
Each uncoated tablet contains :
Dextromethorphan Hydrobromide
Phenylephrine Hydrochloride
Chlorpheniramine Maleate
Excipients
Colour: Tartrazine |
IP
IP
IP |
10mg
5mg
2mg
q.s |
247 |
Diacerein , Glucosamine & Methylsulfonylmet hane Tablets |
Each film coated tablets contains:
Diacerein
GlucosamineSulphate potassium chloride
Eq.to glucosamine
Methylsulfonylmethane
Excipients
Approved colour used |
IP
USP
USP |
50mg
750mg
446mg
250mg |
248 |
Diclofenac & TolperisoneTablets |
Each uncoated sustained releaseTablet contains:
Tolperisone Hydrochloride
Diclofenac Sodium
Excipients
Approved colour used |
IP |
450mg
100mg
q.s. |
249 |
Diclofenac Diethyl amine, methyl Salicylate, linseed Oil &Menthol Gel |
Composition:-
Diclofenac Diethyl amine
Equ. toDiclofenacSodium 1.0%w/w)
Linseed Oil
Methyl Salicylate
Menthol
Benzyl Alcohol
Excipients |
IP
BP
IP
IP
IP |
1.16%w/w
3.0%w/w
10.0%w/w
5.0%w/w
1.0%w/w
q.s. |
250 |
Diclofenac Diethylamine , Thiocolchicoside, Virgin Linseed Oil, Methyl Salicylate & Menthol Gel |
Composition :
Diclofenac Diethylamine
Equ. to Diclofenac Sodium
Thiocolchicoside
Virgin Linseed Oil
Menthol
Methyl Salicylate
Preservative :
Benzyl Alcohol
Gel Base |
IP
IP
BP
IP
IP
IP |
1.16%w/w
1.00%w/w
0.125%w/w
3.0%w/w
5.0%w/w
10%w/w
1.0%w/w
q.s. |
251 |
Diclofenac Paracetamol & Chlorzoxazone Tablets |
Each uncoated tablet contains:-
Paracetamol
Diclofenac Potassium
Chlorzoxazone
Excipients
Colour:-Approved colour used |
IP
BP
USP |
325 mg
50 mg
250mg
q.s. |
252 |
Diclofenac Potassium , Paracetamol & Serratiopeptidase Tablets |
Each film coatedTablet Contains:
Diclofenac Potassium
Paracetamol
Serratiopeptidase
( Eq. to enzyme activityof 20000 units of enteric coated
granules)
Excipients
Approved Colour Used |
BP
IP
IP |
50mg
325mg
10mg
q.s. |
253 |
Diclofenac Potassium , Paracetamol & Serratiopeptidase Tablets |
Each film coatedTablet Contains:
Diclofenac Potassium
Paracetamol
Serratiopeptidase
( Eq. to enzyme activityof 20000 units of enteric coated
granules)
Excipients
Approved Colour Used. |
BP
IP
IP |
50mg
325mg
10mg
q.s. |
254 |
Diclofenac Potassium , Paracetamol & Serratiopeptidase Tablets |
Each film coated Tablet Contains:
Diclofenac Potassium
Paracetamol
Serratiopeptidase
( Eq. to enzyme activityof 30000 units of enteric coated
granules)
Excipients
Approved Colour Used |
BP
IP
IP |
50mg
325mg
15mg
q.s. |
255 |
Diclofenac Potassium & Metaxalone Tablets |
Each uncoated Tablet contains:
Diclofenac Potassium
Metaxalone
Excipients
Approved colour used |
BP |
50mg
400mg
q.s. |
256 |
Diclofenac Potassium & Paracetamol Tablets |
Each film coated Tablet Contains:
Diclofenac Potassium
Paracetamol
Excipients
Approved colour used |
BP
IP |
50mg
325mg
q.s. |
257 |
Diclofenac Potassium & Paracetamol Tablets |
Each film coated Tablet Contains:
Diclofenac Potassium
Paracetamol
Excipients
Approved colour used |
BP
IP |
50mg
325mg
q.s. |
258 |
Diclofenac Potassium & Serratiopeptidase Tablets |
Each film coated tablet contains :
Diclofenac Potassium
Serratiopeptidase
(as enteric coated 20,000 unit of activated enzymatic activity
of Serratiopeptidase )
Excipients
Approved colour used. |
BP
IP |
50mg
10mg
q.s. |
259 |
Diclofenac Potassium & Serratiopeptidase Tablets |
Each film coated Tablet contains:
Diclofenac Potassium
Serratiopeptidase
(Eq. toenzyme activityof 30000units of enteric coated
granules)
Excipients
Approved colour used |
BP
IP |
50mg
15mg
q.s. |
260 |
Diclofenac Potassium & Thiocolchicoside Tablets |
Each enteric coated tablet contains:
Diclofenac Potassium
Thiocolchiside
Excipients
Approved colour used. |
I.P.
I.P. |
50mg
4mg
q.s. |
261 |
Diclofenac Potassium Sustained Release Tablets |
Each film coated sustainedrelease tablet contains:
Diclofenac Potassium
Excipients
Approved colour used |
BP |
100 mg
q.s. |
262 |
Diclofenac Potassium Tablets IP |
Each Filmcoated Tablet contains:
Diclofenac Potassium
Excipients
Approved colour used |
IP |
25mg
q.s. |
263 |
Diclofenac Potassium, Paracetamol & Chlorzoxazone Tablets |
Each film coated Tablet Contains:
Diclofenac Potassium
Paracetamol
Chlorzoxazone
Excipients
Approved colour used |
BP
IP
IP |
50mg
325mg
500mg
q.s. |
264 |
Diclofenac potassium, Paracetamol & Chymotrypsin Tablets (Discontinue AFTER GETTING APPROVAL AS PER S.No.892 which is in enteric coated formulation). |
Each Film coated TabletsContains:
Diclofenac potassium
Paracetamol
Trypsin Chymotrypsin
50000 Armour unit of enzymatic activity
(Supplied by a purified concentrate which has specific Trypsin
and chymotrypsin activity in ratio of Approximate six to one)
Excipients
Approved colour used |
BP
IP |
50 mg
325 mg
50000AU
q.s. |
265 |
Diclofenac Potassium, Paracetamol & Trypsin Chymotrypsin Tablets |
Each enteric coated tablet contains:
Diclofenac Potassium
Paracetamol
Trypsin Chymotrypsin
50000 Armour unit of enzymatic activity.
Excipients
Approved colour used. |
BP
IP
BP |
50mg
325mg
50000AU
q.s. |
266 |
Diclofenac Sodium , Paracetamol & Chlorzoxazone Tablets |
Each uncoated tablet contains:-
Paracetamol
Diclofenac Sodium
Chlorzoxazone
Excipients
Colour:-Approved colour used |
IP
IP
USP |
325 mg
50 mg
250mg
q.s. |
267 |
Diclofenac Sodium & Paracetamol Tablets |
Each film coated tablets contains:
Diclofenac Sodium
(as Enteric coated)
Paracetamol
Excipients
Approved colour used |
IP
IP |
50mg
325mg |
268 |
Diclofenac Sodium & Paracetamol Tablets IP |
Each Uncoated Bilayered tablet contains :
Diclofenac Sodium
Paracetamol
Excipients
Approved colour used. |
IP
IP |
50mg
325mg
q.s. |
269 |
Diclofenac Sodium & Serratiopeptidase Tablets |
Each film coatedTablet Contains:
Diclofenac Sodium
Serratiopeptidase
(Eq. toenzyme activityof 20000 units of enteric coated
granules)
Excipients
Approved Colour Used. |
IP
IP |
50mg
10mg
q.s. |
270 |
Diclofenac Sodium & Thiocolchicoside Capsules |
Each hard gelatin capsule
contain:
Diclofenac Sodium
Thiocolchicoside
Excipients
Approved colour used in emptyhard gelatin capsule |
IP
IP |
50 mg
4 mg
q.s. |
271 |
Diclofenac Sodium SR Tablet IP |
Each film coated Sustained Release tablet Contains
Diclofenac Sodium
Excipients
Colour :-Approved colour used |
IP |
100mg
q.s |
272 |
Diclofenac Sodium Tablets IP |
Each Enteric Coated Tablet Contains:
Diclofenac Sodium
Excipients
Approved Colour Used |
IP |
50mg
q.s |
273 |
Diclofenac, Methyl Salicylate & Menthol Topical Gel |
Diclofenac Diethylamine
Eq. to Diclofenac Sodium
Methyl Salicylate
Menthol
Benzyl Alcohol
(As Preservative)
Gel Base |
IP
IP
IP
IP
IP |
2.32% w/w
2% w/w
10% w/w
5% w/w
1% w/w
q.s |
274 |
Diclofenac, Paracetamol and Serratiopeptidase Tablets |
Each film coated tablet contains:-
Diclofenac Sodium
Paracetamol
Serratiopeptidase
(Eq.toEnzyme activity30000 Units of enteric coated
granules)
Excipients
Colour:-Approved colour used |
IP
IP
IP |
50 mg
325 mg
15 mg
q.s. |
275 |
Dicyclomine Hydrochloride & Activated Dimethicone Drops |
Each ml contains:
Dicyclomine Hydrochloride
Activated Dimethicone
Flavoured syrupybase.
Approved colour used. |
IP
IP |
10mg
40mg
q.s. |
276 |
Dicyclomine Hydrochloride & Simethicone Suspension |
Each 5ml contains:
Dicyclomine Hydrochloride
Simethicone Emulsion USP
Eq. to Simethicone
In a flavoured syrupy base
Approved colour used. |
IP
USP |
10mg
40mg
q.s. |
277 |
Dicyclomine Hydrochloride& Paracetamol Tablets |
Each uncoated Tablet contains:
Dicyclomine Hydrochloride
Paracetamol
Excipients
Approved colour used |
IP
IP |
20mg
500mg
q.s. |
278 |
Dicyclomine Hydrochloride& Simethicone Oral Drops |
Each ml contains :
Dicyclomine Hydrochloride
Simethicone
In a flavoured syrupybase
Approved Coloured used |
IP
IP |
10mg
40mg
q.s |
279 |
Digestive Enzyme Drops. |
Each ml contains:
Alpha amylase (1:800)
Pepsin
Dil oil
Anise oil
Carawayoil
Flavored syrupy base
ApprovedColour Used |
IP
IP
BP
BP
BP |
20mg
10mg
2mg
2mg
2mg
q.s |
280 |
Digestive Enzyme syrup |
Each 5 ml Contains :-
Alpha Amylase(1:1200)
(Fungal digest derived from Asper gillous oryzaedigest not
less than 60gm of cooked starch)
Pepsin (1:3000)
(Digest not lessthan 30gm of coagulated eggalbumen)
In a Flavoured syrupybase.
Approved Colour Used |
IP
IP |
50mg
10mg
q.s. |
281 |
Digoxin Tablets IP |
Each Uncoated Tablet Contains:
Digoxin
Excipients |
IP |
0.25mg
q.s. |
282 |
Digoxin Tablets IP |
Each uncoated Tablet Contains:
Digoxin
Excipients
Approved colour used |
IP |
0.25mg
q.s. |
283 |
Diphenhydramine HCl, Ammonium Chloride, Sodium Citrate &Menthol Syrup |
Each 5ml contains :
Diphenhydramine HCl
Ammonium Chloride
Sodium Citrate
Menthol
Flavoured SyrupyBase
Approved colour used. |
IP
IP
IP
IP |
14.08mg
138mg
57.03mg
1.14mg
q.s. |
284 |
Disodium Hydrogen Citrate Syrup |
Each 5 ml contains :-
Disodium Hydrogen Citrate
In flavoured syrupyBase
Approved Colour Used. |
BP |
1.37gm.
q.s. |
285 |
Disulfiram Tablets |
Each Uncoated Tablet Contains:-
Disulfiram
Excipients
Colour :- Approved colour used |
IP |
200mg
q.s |
286 |
Domperidone DispersibleTablets |
Each uncoated dispersible tablet contains:
Domperidone
Excipients
Approved colour used |
IP |
10mg
q.s |
287 |
Doxofylline ( Sustained Release) & Montelukast Tablets |
Each Filmcoated Bilayered Tablet Contains :
Doxofylline
(as Sustained Release)
Montelukast Sodium
Equ. to Montelukast
Excipients
Approved colour used |
IP
IP |
400mg
10mg
q.s. |
288 |
Doxofylline & Ambroxol Hydrochloride Tablets |
Each Film coated Tablet Contains :
Doxofylline
Ambroxol Hydrochloride
Excipients
Approved colour used |
IP
IP |
400mg
30mg
q.s. |
289 |
Doxofylline Modified Release Tablets |
Each uncoated Modified Release Tablet contains :
Doxofylline
Excipients |
IP |
650mg
q.s. |
290 |
Doxofylline Tablets IP |
Each filmCoatedTablet Contains:-
Doxofylline
Excipients
Colour :-Approved colour used |
IP |
400mg
q.s. |
291 |
Doxofylline Tablets IP |
Each uncoated Tablet Contains :-
Doxofylline
Excipients |
IP |
400mg
q.s. |
292 |
Doxofylline(SR) & Montelukast Sodium Tablets |
Each uncoated tablet contains:
Doxofylline
(As sustainedrelease)
Montelukast Sodium
Eq. to Montelukast
Excipients
Approved colour used |
IP
IP |
400 mg
10 mg
q.s. |
293 |
Doxycycline & Lactic Acid Bacillus Capsule |
Each hard gelatin capsule contains Doxycycline Lactic Acid Bacillus Excipients Approved colour used in emptycapsule shells. |
IP |
100mg 5 Million q.s. |
294 |
Doxycycline & Lactic Acid Bacillus Tablets |
Each Film coated Tablet Contains :
Doxycycline Hyclate
Equ. To
DoxycyclineLactic
Acid Bacillus
Excipients
Approved colour used |
IP |
100mg
5 Billion Spores
q.s. |
295 |
Doxycycline & Lacticacid Bacillus Capsules |
Each hard gelatin capsules contains :
Doxycycline Hydrochloride
Equ. to Doxycycline
Lactic acid Bacillus
Excipients
Approved Colour used in Emptycapsules Shells. |
IP |
100mg
5Million
q.s |
296 |
Doxycycline Hyclate Capsule USP |
Each hard gelatin capsule contains:
Doxycycline Hyclate
Equ. to Doxycycline
Excipients
Approved colour used in emptycapsule shells |
USP |
100mg
q.s. |
297 |
Doxycycline Hyclate Tablets |
Each film coated Tablet Contains:
Doxycycline Hyclate
Equ. to Doxycycline
Excipients
Approved colour used. |
IP |
100mg
q.s. |
298 |
Doxylamine Succinate & Pyridoxine HCl Tablets |
Each enteric coated tablet contains :
Doxylamine Succinate
Pyridoxine Hydrochloride
Excipients
Approved colour used |
USP
IP |
10mg
10mg
q.s |
299 |
Doxylamine succinate, Pyridoxine hydrochloride & Folicacid Tablets |
Each enteric coated tablets contains:
Doxylamine succinate
Pyridoxinehydrochloride
Folic acid
Excipients
Approved colour used |
USP
IP
IP |
20 mg
20 mg
5 mg
q.s. |
300 |
Doxylamine succinate, Pyridoxine hydrochloride & FolicacidTablets |
Each entericcoatedtablets contains:
Doxylamine succinate
Pyridoxinehydrochloride
Folic acid
Excipients
Approved colour used |
BP
IP
IP |
10 mg
10 mg
2.5 mg
q.s. |
301 |
Dried Aluminium Hydroxide , Magnesium Hydroxide, Simethicone & Sorbitol Oral Suspension |
Each 5ml contains :
Dried Aluminium Hydroxide Gel
Magnesium Hydroxide
Activated Simethicone
Sorbitol Solution (Non Crystallizing 70%)
In a flavoured non syrupy base.
Approved colour used |
IP
IP
IP
IP |
250mg
250mg
50mg
1.25gm
q.s. |
302 |
Dried Aluminium Hydroxide Gel , Magnesium Hydroxide Gel, Oxetacaine & Activated Dimethicone oral Suspension |
Each 5ml contains :
Dried Aluminium Hydroxide Gel
Magnesium Hydroxide Gel
Oxetacaine
Activated Dimethicone
In a Flavoured non syrupybase
Approved colour used |
IP
IP
IP
IP |
300mg
250mg
10mg
50mg
q.s. |
303 |
Dried Aluminium Hydroxide Gel, Magnesium hydroxide, Oxetacaine and Simethicone Suspension |
Each 5ml contain:
Dried Aluminium Hydroxidegel
Magnesium hydroxide
Oxetacaine
Simethicone
In a flavoured sorbitol base
Approved colour used |
IP
IP
BP
IP |
600 mg
300mg
10 mg
25 mg
q.s. |
304 |
Dried Aluminium Hydroxide, Magnesium Aluminium Silicate Hydrate, Magnesium Hydroxide & Simethicone Chewable Tablets |
Each uncoated Chewable Tablet Contains:
Dried Aluminium Hydroxide
Magnesium Aluminium Silicate Hydrate
Magnesium Hydroxide
Simethicone
Excipients
Colour: Erythrosine & Ponceau 4R |
IP
IP
IP |
300mg
50mg
25mg
25mg
q.s |
305 |
Drotaverine hydrochloride & Mefenamic Acid Tablets |
Each film coated tablets:
Drotaverine hydrochloride
Mefenamic Acid
Excipients
Approved colour used |
IP
IP |
80 mg
250 mg
q.s. |
306 |
Drotaverine Hydrochloride Tablet IP |
Each film coated tablet Contains:-
Drotaverine Hydrochloride
Excipients
Colour :-Approved colour used |
IP |
40mg
q.s. |
307 |
Drotaverine Hydrochloride Tablets IP |
Each Film coated Tablet contains
Drotaverine Hydrochloride
Excipients
Colour : Approved Coloured used |
IP |
80mg
q.s |
308 |
Drotaverine Hydrochloride Tablets IP |
Each uncoated Tablet contains
Drotaverine Hydrochloride
Excipients
Approved Coloured used |
IP |
80mg
q.s |
309 |
Duloxetine Gastro- resistant Tablets IP |
Each enteric coated Tablet contains :
Duloxetine Hydrochloride
Equ. to Duloxetine
Excipients
Approved Colour used. |
IP |
20mg
q.s. |
310 |
EbastineTablet IP |
Each film coated tablet contains:
Ebastine
Excipients
Approved colour used |
IP |
10 mg
q.s |
311 |
EbastineTablet IP |
Each film coated tablet contains:
Ebastine
Excipients
Approved colour used |
IP |
20 mg
q.s |
312 |
Elemental Iron , Elemental zinc &folic Acid Capsules |
Each hardgelatin Capsule contains:
Elemental Iron
(In the form of Carbonyl Iron )
Zinc Sulphate Monohydrate
Equ. to Elemental Zinc
Folic Acid
Excipients
Colour: - Approved colour used in hard Gelatin Capsule &
shells. |
IP
IP |
50mg
61.8mg
22.5mg
0.5mg |
313 |
Empagliflozin & Linagliptin Tablets |
Each film coated tablet contains:-
Empagliflozin
Linagliptin
Excipients
Approved colour used . |
|
10mg
5mg
q.s. |
314 |
Empagliflozin & Linagliptin Tablets |
Each film coated tablet contains:-
Empagliflozin
Linagliptin
Excipients
Approved colour used . |
|
25mg
5mg
q.s. |
315 |
Enteric coated Esomeprazole 40mg & Itopride Hydrochloride Sustained Release 150mg Capsules |
Each hard gelatin capsule contains:
Esomeprazole Magnesium Trihydrate
Eq.to Esomeprazole
(AsEntericCoated Pellets)
Itopride Hydrochloride
(In Sustained ReleaseForm)
Excipients
Approved colour used. |
IP
IP |
40mg
150mg
q.s. |
316 |
Ergotamine Tartrate, Caffeine, Paracetamol & Prochlorperazine Maleate Tablets |
Each uncoated tablet contain:
Ergotamine Tartrate
Caffeine (Monohydrate)
Paracetamol
Prochlorperazine Maleate
Excipients
Approved colour used
(Banned drug 12/08/2024) |
IP
IP
IP
IP |
1 mg
100 mg
250 mg
2.5 mg
q.s |
317 |
Erythromycin StearateTablet IP |
Each film coated Tablet Contains:
Erythromycin Stearate
Equ. toErythromycin
Excipients
Colour:- Approved colour used |
IP |
250mg |
318 |
Escitalopram Oxalate & Clonazepam Tablet IP |
Each film coated Tablet Contains:-
Escitalopram Oxalate
Equivalent toEscitalopram
Clonazepam
Excipient
Approved colour used |
IP
IP |
10 mg
0.5 mg
q.s. |
319 |
Escitalopram Oxalate Tablet |
Each film coated Tablet Contains:
Escitalopram oxalate
Equ. toEscitalopram
Excipients
Colour : Approved Coloured Used |
IP |
10mg
q.s |
320 |
Esomeprazole (Enteric Coated) & Domperidone Sustained Release Capsules |
Each hard gelatin capsule contains:-
Esomeprazole Magnesium Trihydrate
Equ. to Esomeprazole
(Asa enteric coated Pellets)
Domperidone
(as a Sustainedrelease pellets)
Excipients
Approved colour used in emptycapsule shells. |
IP
IP |
40mg
30mg
q.s |
321 |
Esomeprazole (Enteric-coated) & Levosulpiride(Susta ined-release) Capsules |
Each hard gelatin Capsule contains :
Esomeprazole Magnesium Trihydrate
Equ. to Esomeprazole
(as enteric –coated pellets)
Levosulpiride
(as sustained –release pellets)
Excipients
Colour: Titanium Dioxide IP is used in pellets & approved
colour(s) are used in Emptycapsules shells. |
IP |
40mg
75mg
q.s |
322 |
Esomeprazole Gastro–resistant Tablet IP |
Each Enteric coated Tablet contains :-
Esomeprazole magnesium Trihydrate
Equ. to Esomeprazole
Excipients
Colour : Approved Coloured Used |
IP |
40mg
q.s. |
323 |
Etizolam Tablets |
Each film coated tablet contains:
Etizolam
Excipients
Approved colour used |
|
0.25 mg
q.s |
324 |
Etizolam Tablets |
Each film coated tablet contains:
Etizolam
Excipients
Approved colour used |
|
0.5 mg
q.s |
325 |
Etodolac Extended Release Tablets USP |
Each Film Coated Extended Release Tablet contains :
Etodolac
Excipients
Approved colour used |
IP |
600mg
q.s. |
326 |
Etodolac Tablets IP |
Each Film Coated Tablet contains:
Etodolac
Excipients
Approved colour used |
IP |
400mg
q.s. |
327 |
Etodolac Tablets IP |
Each Film Coated Tablet contains:
Etodolac
Excipients
Approved colour used |
IP |
300mg
q.s. |
328 |
Etophylline & Theophylline Prolonged Release Tablet IP |
Each Film coated prolonged release Tablet contains
Etophylline
Theophylline Anhydrous
Equ. to Theophyllinehydrate
Excipients
Colour : Approved Coloured Used |
IP
IP |
115mg
35mg
q.s |
329 |
Etoricoxib & Paracetamol Tablets |
Each film coated tablet Contains:-
Etoricoxib
Paracetamol
Excipients
Colour :-Approved colour used |
IP
IP |
60mg
325mg
q.s |
330 |
Etoricoxib & Thiocolchicoside Tablets |
Each film coated tablet Contains:-
Etoricoxib
Thiocolchicoside
Excipients
Colour :-Approved colour used |
IP
IP |
60mg
4mg
q.s |
331 |
Etoricoxib and Pregabalin (Prolonged Release) Tablets |
Each uncoated bilayered tablet contains:
Etoricoxib
Pregabalin
(As prolonged release)
Excipients
Approved colour used. |
IP
IP |
60 mg
75 mg
q.s. |
332 |
Etoricoxib tablets IP |
Each film coated tablet contains:-
Etoricoxib
Excipients
Colour:-Approved Colour Used |
IP |
90 mg
q.s. |
333 |
Etoricoxib tablets IP |
Each film coated tablet contains:-
Etoricoxib
Excipients
Colour:-Approved Colour Used |
IP |
60 mg
q.s. |
334 |
Etoricoxib tablets IP |
Each film coated tablet contains:-
Etoricoxib
Excipients
Colour:- Approved Colour Used |
IP |
120 mg
q.s. |
335 |
Etoricoxib,Linse ed Oil,Methyl Salicylate & Menthol Gel |
Etoricoxib
Linseed Oil
Methyl Salicylate
Menthol |
IP
BP
IP
IP |
1.0% W/W
3.0% W/W
10.0% W/W
5.0% W/W
q.s. |
336 |
Febuxostat Tablet |
Each film coated tablet contains:
Febuxostat
Excipients
Approved colour used |
|
120 mg
q.s |
337 |
FebuxostatTablets |
Each film coated tablet contains:-
Febuxostat
Excipients
Colour:-Approved colour used |
|
40 mg
q.s. |
338 |
FebuxostatTablets |
Each film coated tablet contains:-
Febuxostat
Excipients
Colour:-Approved colour used |
|
80 mg
q.s. |
339 |
Ferric Ammonium Citrate, Folic Acid, Vit. B12 & Zinc Syrup |
Each 15ml contains :
Ferric Ammonium Citrate
Equ. to Elemental Iron
Cyanocobalamin
Folic Acid
ZincSulphate
In a Flavoured SyrupyBase.
Approved Colour Used |
IP
IP
IP
IP |
200mg
41mg
7.5mcg
0.5mg
7mg
q.s. |
340 |
Ferrous Ascorbate , Folic Acid & Zinc Tablet |
Each film coatedTablet Contains:
Ferrous Ascorbate
Equ. toElemental Iron
Folic Acid
Zinc SulphateMonohydrate
Equ. to Elemental Zinc
Excipients
Approved Colour Used. |
IP
IP |
100mg
1.5mg
22.5mg
q.s. |
341 |
Ferrous Ascorbate , Folic Acid, Methylcobalamin & Zinc Sulphate Monohydrate Tablet |
Each FilmCoated Tablet Contains:
Ferrous Ascorbate
Equ. ToElemental
IronFolic Acid
Methylcobalamin
Zinc Sulphate Monohydrate
Equ. To Elemental Zinc
Excipients
Approved Colour Used |
IP
IP
IP
IP |
100mg
1.1mg
1.5mg
22.5mg
q.s. |
342 |
Ferrous Ascorbate (SR) and L-Methylfolate Tablets |
Each film coated tablet contains:
Ferrous Ascorbate
Eq. to Elemental Iron
(In sustained release form)
Calcium L-5 Methyltetrahydrofolate
Eq. to L-Methylfolate
Excipients
Approved colour used.
Appropriate overages of L-Methylfolate added to
compensate loss on storage. |
I.P.
U.S.P
q.s. |
100mg
0.5mg |
343 |
Ferrous Ascorbate & Folic Acid Suspension |
Each 5ml contains:-
Ferrous Ascorbate
eq. toElemental Iron
Folic Acid
Excipients
In flavored syrupybase
ApprovedColour Used |
IP |
30mg
550mcg
q.s. |
344 |
Ferrous Ascorbate & Folic Acid Tablets |
Each film coated tablet contains:-
Ferrous Ascorbate
Eq.toElementalIron
Folic Acid
Excipients
Colour:-Approved colour used |
IP |
100 mg
1.5 mg
q.s. |
345 |
Ferrous Ascorbate, Folic Acid & Methylcobalamin Tablets |
Each film coated tablets contains:
Ferrous Ascorbate
Eq. to Elemental Iron
Folic Acid
Methylcobalamin
Excipients
Approved Colour used.
Appropriate overages of vitamins added to compensate the
loss on storage. |
I.P.
I.P. |
100mg
1.5mg
1500 mcg
qs |
346 |
Ferrous Ascorbate, Folic acid, Cyanocobalamin & Zinc Tablet |
Each film coatedtablet contain:
Ferrous Ascorbate
Equ. toElmental Iron
Folic acid
Zinc Sulphate Monohydrate
Equ. to Elmental Zinc
Cyanocobalamin
Excipients
Approved colour used |
IP
IP
IP |
100 mg
1.5mg
22.5mg
15mcg
q.s |
347 |
Ferrous Ascorbate, Folic Acid, Methylcobalamin Suspension |
Each 5ml contains :
Methylcobalamin
Ferrous Ascorbate
Equ. toElemental Iron
Folic Acid
In a flavoured syrupyBase
Approved colour used. |
IP
IP |
500mcg
30mg
0.5mg
q.s. |
348 |
Ferrous Gluconate, Folic Acid, Vitamin B12, Dibasic Calcium Phosphate & Zinc Sulphate Capsules |
Each hard gelatin capsule contains:
Ferrous Gluconate
Eq. to Elemental Iron
Folic Acid
Vitamin B12
(As gelatin triturate 0.1%)
Dibasic Calcium Phosphate
(Dihydrate)
Zinc Sulphate Excipients
Appropriate overages of vitamins added.
Approved colour used in hard gelatin capsule shell. |
I.P.
I.P.
I.P.
I.P.
I.P. |
259mg
30mg
0.5mg
2.5 mcg
100mg
33mg
q.s. |
349 |
Fexofenadine & Montelukast ChewableTablets |
Each Uncoated Chewable Tablet Contains :
Fexofenadine Hydrochloride
Montelukast Sodium
Equ. to Montelukast
Excipients |
IP
IP |
120mg
10mg
q.s. |
350 |
Fexofenadine & MontelukastTablet |
Each uncoatedTablet contains
Fexofenadine Hydrochloride
Equ. to Fexofenadine
Montelukast Sodium
Equ. toMontelukast
Excipients
Colour : ApprovedColour Used |
IP
IP |
120mg
10mg
q.s. |
351 |
Fexofenadine Hydrochloride & Montelukast Tablets |
Each film coated tablet contains:
Fexofenadine Hydrochloride
Montelukast sodium
Equ. to Montelukast
Excipients
Approved colour used. |
IP
IP |
120mg
10mg
q.s. |
352 |
Fexofenadine Hydrochloride Tablet IP |
Each uncoatedTablet contains
Fexofenadine Hydrochloride
Equ. to Fexofenadine
Excipients
Colour : ApprovedColour Used |
IP |
120mg
q.s |
353 |
Fexofenadine Hydrochloride Tablets IP |
Each FilmcoatedTabletsContains:
Fexofenadine Hydrochloride
Excipients
Approved colour used |
IP |
180 mg
q.s. |
354 |
Fexofenadine Hydrochloride Tablets IP |
Each film coated tablet contains:
Fexofenadine Hydrochloride
Excipients
Approved colour used. |
IP |
120mg
q.s |
355 |
Flavoxate Tablet IP |
Each film coated tablet contains:
Flavoxate
Excipients
Approved colour used |
IP |
200 mg
q.s |
356 |
Fluconazole Tablet IP |
Each Uncoated Tablet Contains: -
Fluconazole
Excipients
Colour : -ApprovedColour used |
IP |
150mg
q.s. |
357 |
Fluconazole Tablets IP |
Each uncoated tablet Contains:
Fluconazole
Excipients
Approved colour used |
IP |
400mg
q.s. |
358 |
FluconazoleTablets IP |
Each uncoated tablets contains:
Fluconazole
Excipients
Approved colour used |
IP |
200 mg
q.s. |
359 |
Flunarizine Tablets |
Each Uncoated Tablet Contains:
Flunarizine
(as Flunarizine Dihydrochloride)
Excipients
Approved colour used |
BP |
5mg
q.s. |
360 |
Flunarizine Tablets IP |
Each uncoated Tablet contains
Flunarizine Hydrochloride
Excipients
Approved Coloured used |
BP |
10mg
q.s |
361 |
Fluoride Medicated Oral Gel |
Composition :
Sodium Monofluorophosphate
In a Flavoured Gel base
Approved Colour used |
USP |
0.35%w/w
q.s |
362 |
Fluoxetine & Alprazolam Tablets |
Each uncoated tablet contains:
Fluoxetine Hydrochloride
Eq. to fluoxetine
Alprazolam
Excipients
Approved colour used |
IP
IP |
20 mg
0.25 mg
q.s |
363 |
Fluoxetine Capsules IP |
Each hard gelatin Capsule contains :
Fluoxetine Hydrochloride
Equ. to fluoxetine
Excipients
Approved colour used |
IP |
20mg |
364 |
FluoxetineTablet IP |
Each film coated tablet Contains:-
Fluoxetine Hydrochloride
Equ. toFluoxetine
Excipients
Colour :-Approved colour used |
IP |
20mg
q.s. |
365 |
Flupentixol Dihydrochloride & Melitracen Hydrochloride Tablets |
Each film coated tablet contains :
Flupentixol Dihydrochloride
Equ. to Flupentixol
Melitracen Hydrochloride
Equ. to Melitracen
Excipients
Approved colour used. |
BP |
0.5mg
10mg
q.s |
366 |
Flupirtine Maleate Capsules |
Each hard gelatin capsules contains :
Flupirtine Maleate
Excipients
Approved colour used in EmptyCapsule Shells |
|
100mg
q.s. |
367 |
Fluticasone Propionate Cream I.P |
Each g contains
Fluticasone
PropionateExcipients |
IP |
0.05% w/w
q.s. |
368 |
Folic Acid Tablets IP |
Each uncoated Tablet Contains:
Folic Acid
Excipients
Approved Colour used |
IP |
10mg
q.s |
369 |
Folic Acid Tablets IP |
Each uncoated Tablet Contains:
Folic Acid
Excipients
Approved Colour used |
IP |
5mg
q.s |
370 |
Folic Acid, Methylcobalamin, Pyridoxine Hydrochloride & Docosahexaenoic Acid Capsules |
Each hard gelatin capsule contains:
Folic Acid
Methylcobalamin
Pyridoxine Hydrochloride
Docosahexaenoic Acid
Powder (10%w/w)
Appropriate overages of vitamins are added to compensate
the loss on storage. |
IP
IP
IP |
5mg
1500mcg
1.5mg
200mg
q.s. |
371 |
Frusemide Tablets IP |
Each uncoated tablet contains:
Frusemide
Excipients
Approved colour used. |
IP |
40mg
q.s. |
372 |
Fungal Diastase & Pepsin Drops |
Each ml contains:
Diastase (1: 1200)
(Fungal Diastase derived from Aspergillus oryzae, digest not
less than 40g cooked starch)
Pepsin (1: 3000)
(Digest not less than 15g of coagulated egg Albumin)
Flavoured syrupybase
Approved colour used |
IP
IP |
33.33mg
5mg
q.s. |
373 |
Fungal Diastase & Pepsin Syrup |
Each 15ml contains :
Fungal Diastase(1:1200)
Pepsin (1:3000)
In a flavoured syrupyBase
Approved colour used |
IP
IP |
50mg
10mg
q.s. |
374 |
Furosemide Tablets IP |
Each Uncoated Tablet Contains:
Furosemide
Excipients |
IP |
40mg
q.s. |
375 |
Fusidic Acid & Beclomethasone Dipropionate Cream |
Composition :
Fusidic Acid
Beclomethasone Dipropionate
Preservatives
Chlorocresol
In a water Miscible cream Base |
IP
IP
IP |
2.00%w/w
0.025%w/w
0.12%w/w
q.s |
376 |
Fusidicacid Cream IP |
Composition:
Fusidic Acid
Cream Base |
IP |
2%w/w
q.s. |
377 |
Gabapentin & Methylcobalamin Tablet |
Each film coated tablet contains;
Gabapentin
Methylcobalamine
Excipients
Approved colour used |
IP
IP |
300mg
500mcg
q.s |
378 |
Gabapentin & Methylcobalamin Tablets |
Each film coated Tablet Contains:
Gabapentin
Methylcobalamin
Excipients
Approved colour used. |
IP
IP |
100mg
500mcg
q.s. |
379 |
Gabapentin and Nortriptyline Tablets |
Each film coated Tablet contains:
Gabapentin
Nortriptyline Hydrochloride
Equ. to Nortriptyline
Excipients
Approved colour used |
IP
IP |
300mg
10mg
q.s |
380 |
Gabapentin Tablet IP |
Each film coated tablet contains:
Gabapentin
Excipients
Approved colour used |
IP |
100 mg
q.s |
381 |
Gabapentin Tablet IP |
Each film coated tablet contains:
Gabapentin
Excipients
Approved colour used |
IP |
400 mg
q.s |
382 |
Gabapentin Tablet IP |
Each film coated tablet contains:
Gabapentin
Excipients
Approved colour used |
IP |
800 mg
q.s |
383 |
Gliclazide & Metformin Hydrochloride(SR) Tablets |
Each Uncoated Bilayered Tablet Contains:
Gliclazide
Metformin Hydrochloride
(as Sustained Release)
Excipients
Colour : Approved Coloured used |
IP
IP |
80mg
500mg
q.s. |
384 |
Glimepiride & Metformin Hydrochloride (SR) Tablets |
Each uncoated Bilayered Tablet contains:
Glimepiride
Metformin Hydrochloride
(as Sustained Release form)
Excipients
Approved colour used |
IP
IP |
3mg
500mg
q.s. |
385 |
Glimepiride & Metformin Hydrochloride (SR) Tablets |
Each uncoated Bilayered Tablet contains:
Glimepiride
Metformin Hydrochloride
(as Sustained Release form)
Excipients
Approved colour used |
IP
IP |
4mg
1000mg
q.s. |
386 |
Glimepiride & Metformin Hydrochloride (Sustained Release) Tablets |
Each uncoated Bilayered Tablet contains:
Glimepiride
Metformin Hydrochloride
( as Sustained Release)
Excipients
Approved colour used. |
IP
IP |
3mg
1000mg
q.s. |
387 |
Glimepiride and Metformin Hydrochloride (Sustained Release) Tablets IP |
Each uncoated Bilayered tablet contains:
Glimepiride
Metformin Hydrochloride
(as sustained release)
Excipients
Approved colour used. |
IP
IP |
1mg
1000mg
q.s. |
388 |
Glimepiride, Metformin Hydrochloride (ER) & Voglibose Tablets |
Each uncoated Bilayered Tablet Contains :
Glimepiride
Metformin Hydrochloride
(as Extended Release)
Voglibose
Excipients
Approved colour used |
IP
IP
IP |
1mg
500mg
0.3mg
q.s. |
389 |
GlimepirideTablet IP |
Each uncoated tablet contains:
Glimepiride
Excipients
Approved colour used |
IP |
1 mg
q.s. |
390 |
GlimepirideTablet IP |
Each uncoated tablet contains:
Glimepiride
Excipients
Approved colour used |
IP |
2 mg
q.s. |
391 |
Granisetron Syrup |
Each 5ml contains :
Granisetron Hydrochloride
Equ. to Granisetron
In a Flavoured SyrupyBase. |
BP |
1mg
q.s |
392 |
Griseofulvin Tablets IP |
Each Uncoated Tablet Contains:
Griseofulvin
Excipients |
IP |
500mg
q.s. |
393 |
Griseofulvin Tablets IP |
Each uncoated Tablet Contains:
Griseofulvin
Excipients
Approved Colour Used |
IP |
250mg
q.s |
394 |
Haloperidol Tablet IP |
Each Uncoated Tablet Contains:
Haloperidol
Excipients |
IP |
5mg
q.s. |
395 |
Hydoxychloroquine Tablets IP |
Each film coatedtablets contain:
Hydroxychloroquine Sulphate
Excipients |
IP |
200 mg
q.s. |
396 |
Hydoxychloroquine Tablets IP |
Each film coatedtablets contain:
Hydroxychloroquine Sulphate
Excipients |
IP |
400 mg
q.s. |
397 |
Hydrochlorothiazid e tablet IP |
Each film coated tablet contains:-
Hydrochlorothiazide
Excipients
Colour : Approved Colour Used |
IP |
25mg
q.s |
398 |
Hydrochlorothiazid e tablet IP |
Each film coated tablet contains:-
Hydrochlorothiazide
Excipients
Colour : Approved Colour Used |
IP |
50mg
q.s |
399 |
Hydroquinone, Tretinoin & Fluocinolone Acetonide Cream |
Each 1gcontain:
Hydroquinone
Tretinoin
Fluocinolone Acetonide
In a cream Base |
USP
USP
IP |
20 mg
0.25 mg
0.1 mg
q.s. |
400 |
Hydroxyzine Hydrochloride Tablet |
Each uncoated tablet contains
Hydroxyzine Hydrochloride
eq. to Hydroxyzine
Excipients
Colour :- Approved Colour Used |
IP |
10mg
q.s. |
401 |
Hydroxyzine Hydrochloride Tablet |
Each uncoated tablet contains
Hydroxyzine Hydrochloride
eq. to Hydroxyzine
Excipients
Colour :- Approved Colour Used |
IP |
25mg
q.s. |
402 |
Hydroxyzine Hydrochloride Tablets IP |
Each Film Coated Tablet Contains:
Hydroxyzine Hydrochloride
Excipients
Approved colour used. |
IP |
25mg
q.s |
403 |
Hyoscine Butylbromide IP |
Each Film coated Tablet Contains :
Hyoscine Butylbromide
Excipients
Approved colour used. |
IP |
10mg
q.s. |
404 |
Ibuprofen & Paracetamol Suspension |
Each 5ml Contains
Ibuprofen
Paracetamol
Flavoured Palatable base
Colour : Sunset Yellow FCF |
IP
IP |
100mg
162.5mg
q.s |
405 |
Ibuprofen & Paracetamol Tablets |
Each uncoated Tablet Contains
Ibuprofen
Paracetamol
Excipients
Approved Colour Used |
IP
IP |
400mg
325mg
q.s |
406 |
Ibuprofen Tablets IP |
Each film coated Tablet contains:
Ibuprofen
Excipients
Approved colour used |
IP |
200mg |
407 |
Ibuprofen Tablets IP |
Each film coated Tablet contains:
Ibuprofen
Excipients
Approved colour used |
IP |
400mg |
408 |
Iron &FolicAcid Syrup |
Each 15ml Contains :
Iron(III) Hydroxide Polymaltose Complex
Equ. to Elemental Iron
Folic Acid
In a Flavoured SyrupyBase
Approved colour used. |
IP |
50mg
0.5mg
q.s. |
409 |
Isosorbide Dinitrate Tablets IP |
Each Uncoated Tablet Contains:
Isosorbide Dinitrate
Excipients
Approved colour used |
IP |
5mg
q.s. |
410 |
Isoxsuprine Tablets (Sustained Release) |
Each uncoated Sustained Release Tablet Contains
Isoxsuprine Hydrochloride
Excipients
Approved colour used |
IP |
40mg
q.s |
411 |
Itopride Hydrochloride Sustained Release Capsule |
Each Hard Gelatin Capsule Contains:
Itopride Hydrochloride
(as Sustained Release Pellets)
Excipients
Approved colour used in Emptycapsule Shells. |
|
150mg
q.s. |
412 |
Itraconazole & TerbinafineCream |
Composition :
Itraconazole
Terbinafine Hydrochloride
Preservative :
Methyl Paraben
Phenoxyethanol
Cream base |
BP
IP
IP
IP |
1.0%w/w
1.0%w/w
0.16%w/w
0.05%w/w
q.s. |
413 |
Itraconazole Capsules |
Each hard gelatin capsule contains:-
Itraconazole
Excipients
Approved colour used in emptycapsule shells |
BP |
100mg
q.s |
414 |
Itraconazole Capsules |
Each hard gelatin capsule contains:-
Itraconazole
Excipients
Approved colour used in emptycapsule shells. |
BP |
200mg
q.s |
415 |
Itraconazole Capsules |
Each hard gelatin capsule contains:-
Itraconazole
Excipients
Approved colour used in emptycapsule shells. |
USP |
100mg
q.s |
416 |
Itraconazole Capsules |
Each hard gelatin capsule contains:-
Itraconazole
Excipients
Approved colour used in emptycapsule shells. |
USP |
200mg
q.s |
417 |
Itraconazole Capsules BP |
Each HPMC capsules Contains:
Itraconazole (as Pellets)
Excipients
Approved colour used in Empty capsule Shells.
(Itraconazole Finished Product and Raw Material in IP 2022) |
BP |
200mg
q.s. |
418 |
Itraconazole Cream 1% w/w |
Composition
Itraconazole
Methyl Paraben
Propyl Paraben
In cream base |
BP
IP
IP |
BP
IP
IP1 % w/w
0.1% w/w
0.05% w/w
q.s. |
419 |
Itraconazole Gel |
Composition
Itraconazole
Methyl Paraben
Propyl Paraben
In Gel base |
BP
IP
IP |
1 % w/w
0.1% w/w
0.05% w/w
q.s. |
420 |
Ivermactin Tablet IP |
Each uncoated tablet contains:
Ivermactin
Excipients
Approved colour used |
IP |
6 mg
q.s |
421 |
Ivermactin Tablet IP |
Each uncoated tablet contains:
Ivermactin
Excipients
Approved colour used |
IP |
12 mg
q.s |
422 |
Ivermectin & Albendazole Tablets |
Each uncoated tablet contains:
Ivermactin
Albendazole
Excipients
Approved colour used |
IP
IP |
12 mg
400mg
q.s |
423 |
Ketoconazole Anti- Dandruff Shampoo |
Composition:
Ketoconazole
Conditioner Shampoo Base |
IP |
2.0%w/v
q.s |
424 |
Ketoconazole Cream |
Composition :
Ketoconazole
Preservatives:
Methyl Paraben
Phenoxyethanol
Cream Base |
IP
IP
IP |
2.0%w/w
0.1%w/w
0.05%w/w
q.s |
425 |
Ketoconazole Lotion |
Composition :
Ketoconazole
In a perfumed conditioner
Lotion Base
Approved Colour used |
IP |
2.0%W/V
q.s |
426 |
Ketoconazole Tablet IP |
Each uncoated tablet contain:
Ketoconazole
Excipients
Approved colour used |
IP |
200 mg
q.s |
427 |
Ketoconazole Zinc Pyrithione Shampoo |
Composition :
Ketoconazole
Zinc Pyrithione (ZPTO)
Conditioner Shampoo Base
Colour: Erythrosine |
IP |
2.0%w/v
1.0%w/v
q.s |
428 |
Ketrolac Tromethamine DispersibleTablets |
Each uncoated dispersible tablets contains:
Ketrolac Tromethamine
Excipients
Approved colour used |
IP |
10 mg
q.s. |
429 |
L- Carnitine , L- Tartrate, Folic Acid & Methylcobalamin Tablets |
Each film coated Tablet contains:
L-Carnitine L-Tartrate
Equ. to L-Carnitine
Methylcobalamin
Folic Acid
Excipients
Approved colour used |
IP
IP |
500mg
1500mcg
1.5mg
q.s. |
430 |
L- Lysine with Multivitamin & Multimineral Syrup |
Each 5ml contains :
ZincSulphate
Nicotinamide
L-Lysine Hydrochloride
D- Panthenol
Thiamine Hydrochloride
Riboflavin Sodium Phosphate
Pyridoxine Hydrochloride
Copper Sulphate
Potassium Iodide
Sodium Selenite Pentahydrate
Equ. to Selenium
Cyanocobalamin
Vitamin “A”(as Palmitate )
Cholecalciferol
Vitamin “E” Acetate
PleasantlyFlavoured SyrupyBase.
Approved colour used. |
IP
IP
USP
IP
IP
IP
IP
BP
IP
IP
IP
IP
IP |
22.5mg
7.5mg
5mg
1.25mg
0.75mg
0.75mg
0.5mg
100mcg
50mcg
10mcg
0.5mcg
1250IU
100IU
2.5IU
q.s. |
431 |
L-Arginine & Proanthocynadine Granules Sachet |
Each 5 gm sachet contain:
L-Arginine
Proanthocynadine
Excipients
Approved colour used |
IP |
3.0 gm
75 mg
q.s. |
432 |
L-Carnitine L- Tartrate, Methylcobalamin and Folic Acid Tablets |
Each FilmCoated Tablet Contains:
L-Carnitine L-Tartrate
Methylcobalamin
FolicAcid
Excipients
Approved colour used. |
IP
IP |
500mg
1500mcg
1.5mg
q.s. |
433 |
L-Mehtylfolate, Methylcobalamin & Pyridoxal-5-Phosphate Tablets |
Each film coated tablet contains:
Calcium L-5 Methyltetrahydrofolate
Equivalent to L-Methylfolate
Methylcobalamin
Pyridoxal-5-Phosphate
Excipients
Approved colour used
Appropriate overages of vitamins added to compensate the
possible loss on storage. |
U.S.P.
I.P. |
5 mg
1500 mcg
0.5 mg
q.s. |
434 |
L-methylfolate Calcium, Methylcobalamin, Pyridoxal-5-Phosphate Tablets |
Each film coated tablet contains:-
L-methylfolate
Methylcobalamin
Pyridoxal-5-Phosphate
Excipients
Approved colour used . |
IP |
1mg
1500mcg
0.5mg
q.s. |
435 |
Labetalol Tablets IP |
Each film coated Tablet Contains:
Labetalol Hydrochloride
Excipients
Approved colour used. |
IP |
50mg
q.s |
436 |
Labetalol Tablets IP |
Each film coated Tablet Contains:
Labetalol Hydrochloride
Excipients
Approved colour used. |
IP |
100mg
q.s |
437 |
Lactulose Solution USP |
Each 15 ml contain:
Lactulose
In flavoured Syrupybase
Approved colour used |
USP |
10 gm.
q.s. |
438 |
LactuloseSolution USP |
Each 15ml contain:
Lactulose
In flavoured Syrupybase
Approved colour used |
USP |
10 mg
q.s. |
439 |
Lansoprazole orally Disintegrating Tablets |
Each uncoated tablet contains:
Lansoprazole
(as enteric coated pellets)
Excipients
Approved colour used |
IP |
15 mg
q.s. |
440 |
Lansoprazole Orally Disintegrating Tablets 30mg |
Each uncoated orallyDisintegrating tablet contains:
Lansoprazole
(As enteric coated pellets)
Excipients
Approved colour used. |
IP |
30mg
q.s. |
441 |
Leflunomide Tablet IP |
Each film coated Tablet Contains:
Leflunomide
Excipients
Colour : Approved Coloured Used |
IP |
20mg
q.s |
442 |
Leflunomide Tablet IP |
Each film coated Tablet Contains:
Leflunomide
Excipients
Colour : Approved Coloured Used |
IP |
10mg
q.s |
443 |
Letrozole Tablets USP |
Each film coated Tablet contains:
Letrozole
Excipients
Approved colour used. |
USP |
2.5mg
q.s. |
444 |
Levetiracetam Tablet IP |
Each film Coated Tablet Contains :-
Levetiracetam
Excipients
Colour :- Approved colour used |
IP |
250mg
q.s |
445 |
Levetiracetam Tablet IP |
Each film Coated Tablet Contains :-
Levetiracetam
Excipients
Colour :- Approved colour used |
IP |
500mg
q.s |
446 |
Levocarnitine Oral Solution U.S.P. |
Each 5ml contains:
Levocarnitine
In a flavoured syrupy base
Approved colour used. |
I.P. |
500mg |
447 |
Levocetirizine & Montelukast Suspension |
Each 5ml Contains :
Levocetirizine Hydrochloride
Montelukast Sodium
Equ. to Montelukast
In a flavoured syrupybase.
Approved colour used |
IP
IP |
2.5mg
4mg
q.s. |
448 |
Levocetirizine Dihydrochloride & Montelukast DispersibleTablets |
Each uncoated dispersible Tablet contains :
Levocetirizine Dihydrochloride
Montelukast sodium
Equ. to Montelukast
Excipients |
IP
IP |
2.5mg
4mg
q.s |
449 |
Levocetirizine Dihydrochloride & Montelukast Sodium Syrup |
Each 5ml Contains:-
LevocetirizineDihydrochloride
Montelukast Sodium
Equivalent to Montelukast
In flavoured Syrupybase
Approved colour used |
IP
IP |
2.5 mg
4 mg
q.s. |
450 |
Levocetirizine Dihydrochloride Syrup |
Each 5 ml contains:
LevocetirizineDihydrochloride
In a flavoured syrupy base
Approved colour base |
IP |
2.5 mg
q.s. |
451 |
Levocetirizine Dihydrochloride Tablets IP |
Each Uncoated Tablet Contains:-
Levocetirizine Dihydrochloride
Excipients
Colour :-Approved colour used |
IP |
5mg
q.s. |
452 |
Levocetirizine Dihydrochloride Tablets IP |
Each film Coated Tablet Contains :
Levocetirizine Dihydrochloride
Excipients
Approved colour used. |
IP |
5mg
q.s. |
453 |
Levocetirizine Dihydrochloride, Phenylephrine Hydrochloride & Paracetamol Tablets |
Each uncoated Tablet contains :
Levocetirizine Dihydrochloride
Phenylephrine Hydrochloride
Paracetamol
Excipients
(Banned drug 12/08/2024)
(Banned drug 12/08/2024) |
IP
IP
IP |
2.5mg
10mg
500mg
q.s. |
454 |
Levocetirizine Dihydrochloride& Ambroxol Hydrochloride Syrup |
Each 5ml Contains:
LevocetirizineDihydrochloride
Ambroxol Hydrochloride
Flavoured Syrupy Base
Colour : Tartrazine |
IP
IP |
2.5mg
30mg
q.s |
455 |
Levocetirizine HCl, Ambroxol HCl, Guaiphenesin & Menthol Syrup |
Each 5ml Contains :
Levocetirizine Hydrochloride
Ambroxol Hydrochloride
Guaiphenesin
Menthol
In a Flavoured syrupyBase.
Approved Colour Used |
IP
IP
IP
IP |
2.5mg
15mg
50mg
1mg
q.s. |
456 |
Levocetirizine Hydrochloride & Ambroxol Hydrochloride Syrup |
Each 5ml contains:
Ambroxol Hydrochloride
Levocetirizine Hydrochloride
In a flavoured Syrupy Base
Approved colour Used. |
IP
IP |
30mg
5mg
q.s. |
457 |
Levocetirizine Hydrochloride & Ambroxol Hydrochloride Tablet |
Each film coated Tablet contains:
Levocetirizine Hydrochloride
Ambroxol Hydrochloride
Excipients
Approved colour used. |
IP
IP |
5mg
60mg
q.s. |
458 |
Levocetirizine Hydrochloride Tablets IP |
Each Film coated Tablet Contains :
Levocetirizine Hydrochloride
Excipients
Approved colour Used. |
IP |
10mg
q.s. |
459 |
Levocloperastine Fendizoate Oral Suspension |
Each 5ml Contains :
Levocloperastine Fendizoate
Equ. To Levocloperastine
HClIn a Flavoured Syrupy Base
Approved colour used |
|
35.4mg
20mg
q.s. |
460 |
Levodopa & Carbidopa Tablets IP |
Each Uncoated Tablet Contains:
Carbidopa
Equ.ToCarbidopa
AnhydrousLevodopa
Excipients
Approved colour used |
IP
IP |
25mg
250mg
q.s. |
461 |
Levodropropi zine Syrup |
Each 5ml contains:
Levodropropizine
In a flavoured sugar freebase
Approved colour used |
IP |
30mg
q.s. |
462 |
Levodropropizine & Chlorpheniramine maleate Syrup |
Each 5ml contains:-
Levodropropizine
Chlorpheniramine maleate
In a flavoured syrupy base
Approved colour used . |
IP
IP |
30mg
2mg
q.s. |
463 |
Levofloxacin & Ornidazole Oral Suspension |
Each 5ml Contains :
Levofloxacin Hemihydrate
Equ. to Levofloxacin
Ornidazole
In a flavoured SyrupyBase.
Approved colour used |
IP
IP |
125mg
125mg
q.s. |
464 |
Levofloxacin & OrnidazoleTablets |
Each film coated tablets contains:
Levofloxacin hemihydrate
Equivanent to Levofloxacin anhydrous
Ornidazole
Excipients
Approved colour used |
IP
IP |
250 mg
500 mg
q.s. |
465 |
Levofloxacin Oral Solution IP |
Each 5 ml contains:
Levofloxacin Hemhydrate
Eq.to Levofloxacin
Excipients
Approved colour used. |
IP |
125mg
q.s. |
466 |
Levofloxacin Tablets IP |
Each film coated tablet contains:-
Levofloxacin Hemihydrate
Equivalent to Levofloxacin
Excipients
Colour:-Approved colour used |
IP |
250 mg.
q.s. |
467 |
Levofloxacin Tablets IP |
Each film coated tablet contains:-
Levofloxacin Hemihydrate
Equivalent to Levofloxacin
Excipients
Colour:-Approved colour used |
IP |
500 mg.
q.s. |
468 |
Levofloxacin Tablets IP |
Each film coated tablet contains:-
Levofloxacin Hemihydrate
Equivalent to Levofloxacin
Excipients
Colour:-Approved colour used |
IP |
750 mg.
q.s. |
469 |
Levosalbutamol Syrup 1mg/5ml |
Each 5ml contains:
Levosalbutamol Sulphate
Equ. to Levosalbutamol
In a Flavoured SyrupyBase
Approved colour used. |
IP |
1mg
q.s. |
470 |
Levosalbutamol Syrup 2mg/5ml |
Each 5ml contains:
Levosalbutamol Sulphate
Equ. To Levosalbutamol
In a Flavoured SyrupyBase
Approved colour used. |
IP |
2mg
q.s. |
471 |
Levosalbutamol, Ambroxol Hydrochloride & Guaiphenesin Syrup |
Each 5ml Contains :
Levosalbutamol Sulphate
Equ. to Levosalbutamol
Ambroxol Hydrochloride
Guaiphenesin
Flavoured SyrupyBase
Colour: Tartrazine |
IP
IP
IP |
0.5mg
15mg
50mg
q.s |
472 |
Levosulpiride Tablets |
Each Uncoated Tablet Contains:
Levosulpiride
Excipients |
|
25mg
q.s. |
473 |
Levothyroxine sodium Tablets USP |
Each uncoated Tablet Contains:
Levothyroxine Sodium
Equ. to Anhydrous Levothyroxine Sodium
Excipients |
USP |
50mcg
q.s. |
474 |
LinezolidTablet IP |
Each film coated tablet contains:-
Linezolid
Excipients
Colour:-Approved colour used |
IP |
600 mg
q.s. |
475 |
Lipid Based Amphotericin B Gel 0.1% w/w |
Each g contains:
Amphotericin B
Base |
IP |
1.0mg
q.s. |
476 |
Liquid Paraffin & Milk of Magnesia Suspension |
Each15 ml (tablespoonful
133pprox..)Contains:
Liquid Paraffin
Milk ofMagnesia
flavoured syrupy base
Approvedcolour used |
IP
IP |
3.75ml
11.25ml
q.s. |
477 |
Lithium Carbonate Prolonged – Release Tablets IP |
Each uncoated Prolonged-Release tablet contains:
Lithium Carbonate
Excipients
Approved colour used. |
IP |
450mg
q.s. |
478 |
Loperamide Hydrochloride Tablets IP |
Each uncoated tablet contains:-
Loperamide Hydrochloride
Excipients
Colour : Approved Coloured Used |
IP |
2 mg
q.s. |
479 |
Loratadine Tablet USP |
Each uncoated table contains:-
Loratadine
Excipients
Approved colour used |
USP |
10 mg
q.s. |
480 |
Lornoxicam & Paracetamol Tablets |
Each film coatedTablet Contains:-
Lornoxicam
Paracetamol
Excipients
Colour :-Approved colour used |
IP
IP |
4mg
325mg
q.s. |
481 |
Lornoxicam & Paracetamol Tablets |
Each film coatedTablet Contains:-
Lornoxicam
Paracetamol
Excipients
Colour :-Approved colour used |
IP
IP |
8mg
325mg
q.s. |
482 |
Losartan Potassium & Amlodipine Besilate Tablet IP |
Each film coated tablet contains:
Losartan Potassium
Amlodipine Besilate
Eq. to Amlodipine
Excipients
Approved colour used |
IP
IP |
50 mg
5 mg
q.s. |
483 |
Losartan Potassium & Hydrochlorothiazid e Tablet IP |
Each film coated tablet contains:
Losartan Potassium
Hydrochlorothiazide
Excipients
Approved colour used |
IP
IP |
50 mg
12.5 mg
q.s. |
484 |
Losartan Potassium Tablet IP |
Each film coated tablet contains:
Losartan Potassium
Excipients
Approved colour used |
IP |
50 mg |
485 |
Losartan potassium Tablets IP |
Each film coated tablet contains:
Losartan potassium
Excipients
Approved colour used. |
IP |
25mg
q.s |
486 |
Luliconazole cream |
Composition:-
Luliconazole
Preservative Benzyl Alcohal
Cream Base |
IP
IP |
1%w/w
1%w/w
q.s. |
487 |
Luliconazole Cream 1% w/w |
Composition :
Luliconazole
Preservative Benzyl Alcohol
Cream base |
IP |
1%w/w
1%w/w
q.s. |
488 |
Luliconazole Lotion |
Composition :
Luliconazole
Lotion Base |
|
1.0%w/v
q.s |
489 |
Lycopene with Anti-oxidant , Multivitamin & Multimineral Syrup |
Each 10ml Contains:-
Lycopene 6%
Vitamin A Concentrate
(oily form) ( as Palmitate)
Ascorbic Acid (Vitamin C)
Vitamin E acetate
Selenium (Assodium Selenate)
Zinc (As zinc Gluconate)
Manganese(as Manganese Gluconate)
Iodine (as Potassium Iodide )
Copper (as cupric Sulphate)
Thiamine hydrochloride
Riboflavin sodium phosphate
Pyridoxinehydrochloride
In a Flavoured syrupybase.
Approved Colour Used |
IP
IP
IP
USP
USP
IP
USP
IP
IP
IP |
1000mcg
2500IU
50mg
10IU
35mcg
3mg
2mcg
100mcg
500mcg
2mg
3mg
1.5mg
q.s |
490 |
Lycopene with Vitamins & Minerals Syrup |
Each 10ml contains :
Lycopene(10% ) Dispersion
Niacinamide
Pyridoxine Hydrochloride
Cyanocobalamin
Folic Acid
Sodium Selenate
Equ. toElemental Selenium
Zinc Gluconate
Equ. toElemental Zinc
Potassium Iodide
Equ. toavailable Iodine
Cupric Sulfate
Equ. to Elemental Copper
In a Flavoured SyrupyBase.
Approved Colour used. |
USP
IP
IP
IP
IP
USP
IP
USP |
2000mcg
25mg
1.5mg
1mcg
100mcg
35mcg
3mg
100mcg
500mcg
q.s. |
491 |
Magaldrate & Simethicone Oral Suspension IP |
Each 5ml contains :
Magaldrate
(as anhydrous)
Simethicone
In a Flavored Syrupybase
Approved colour used. |
IP
IP |
400mg
60mg
q.s |
492 |
Magaldrate, Simethicone & Domperidone Oral Suspension |
Each 5ml contains:
Magaldrate
Simethicone
Domperidone
Sorbitol Solution (70%)
(Non-Crystallizing)
Approved colour used |
IP
IP
IP
IP |
480mg
20mg
10mg
q.s. |
493 |
Magaldrate, Simethicone & Oxetacaine Suspension |
Each 5ml contains:
Magaldrate
Simethicone
Oxetacaine
Excipients
Approved colour used |
IP
IP
BP |
480mg
20mg
10mg
q.s. |
494 |
Magaldrate, Simethicone & Oxetacaine Suspension. |
Each 5ml contains:
Magaldrate
Simethicone
Oxetacaine
Excipients
Approved colour used. |
IP
IP
BP |
540mg
50mg
10mg
q.s. |
495 |
Magaldrate& Simethicone Oral Suspension |
Each 5ml contains:
Magaldrate
Simethicone
Sorbitol Solution (70%)
(Non Crystallising)
In a flavoured sugar freeBase.
Approved Colour Used. |
IP
IP |
400mg
20mg
q.s. |
496 |
Mecobalamin Tablets |
Each film coated Tablet contains:
Mecobalamin
Excipients
Approved colour used. |
IP |
1500mcg
q.s. |
497 |
Mecobalamin, Alpha Lipoic Acid, Benfotiamine, Folic acid,Chromium Picolinate,Inositol, Pyridoxine HCL, Vitamin D3, & Calcium Carbonate Tablets |
Each film coated tablet contains:
Mecobalamin
Alpha Lipoic Acid
Benfotiamine
Folic acid
Chromium Picolinate
Inositol,
Pyridoxine HCL
Vitamin D3
Calcium Carbonate
Excipients
Approved colour used |
IP
IP
IP
IP
IP
IP
IP
IP |
1500 mcg
100 mg
150 mg
1.5 mg
200 mcg
100 mg
3 mg
1000 IU
500mg
q.s. |
498 |
Mecobalamin, Alpha LipoicAcid, Folic Acid & Pyridoxine Hydrochloride Capsules |
Each hard Gelatin capsule contains :
Mecobalamin
Alpha LipoicAcid
Folic Acid
Pyridoxine Hydrochloride
Excipients
Approved Colour Used |
IP
USP
IP
IP |
1500mcg
100mg
1.5mg
3mg
q.s |
499 |
Mefenamic Acid & Dicyclomine HCl Tablets |
Each uncoated Tablet contains:
Mefenamic Acid
Dicyclomine HCl
Excipients |
IP
IP |
250mg
20mg
q.s |
500 |
Mefenamic Acid & Dicyclomine Tablets IP |
Each uncoated tablet contains:-
Mefenamic Acid
Dicyclomine Hydrochloride
Excipients
Colour:-Approved Colour used |
IP
IP |
250 mg
10 mg
q.s. |
501 |
Mefenamic Acid & Paracetamol Suspension |
Each 5mlContains:-
Mefenamic Acid
Paracetamol
In flavoured Palatablebase
Approved colour used |
IP
IP |
100 mg
250 mg
q.s. |
502 |
Mefenamic Acid & Paracetamol Tablet |
Each uncoated tablet contain:
Mefenamic Acid
Paracetamol
Excipients
Approved colour used |
IP
IP |
500 mg
325 mg
q.s. |
503 |
Mefenamic Acid & Paracetamol Tablets |
Each uncoated tablet contains:
Mefenamic Acid
Paracetamol
Excipients
Approved Colour used |
IP
IP |
250mg
325mg
q.s. |
504 |
Mefenamic Acid Oral Suspension |
Each 5ml contains:
Mefenamic Acid
In a Flavoured SyrupyBase
Approved colour used |
IP |
100mg
q.s. |
505 |
Memantine Hydrochloride & Donepezil Hydrochloride Tablets |
Each film coated tablet contains:
Memantine Hydrochloride
Donepezil Hydrochloride
Excipients
Approved colour used. |
IP
IP |
5mg
5mg
q.s. |
506 |
Mesalamine Prolonged-release Tablets IP |
Each enteric coated Prolonged-release tablet contains:-
Mesalamine
Excipients
Approved colour used . |
IP |
1200mg
q.s. |
507 |
Metformin Hydrochloride (Prolong Release) and Glimepiride Tablet IP |
Each uncoated bilayer tablet contains:-
Metformin Hydrochloride
(Prolonged Release)
Glimepiride
Excipients
Colour:- Approved Colour Used |
IP
IP |
500 mg
1 mg
q.s. |
508 |
Metformin Hydrochloride (Prolong Release) and Glimepiride Tablet IP |
Each uncoated bilayer tablet contains:-
Metformin Hydrochloride
(Prolonged Release)
Glimepiride
Excipients
Colour:- Approved Colour Used |
IP
IP |
500 mg
2 mg
q.s. |
509 |
Metformin Hydrochloride (SR) & Glimepiride Tablets IP |
Each Uncoated Bilayered Tablet Contains:
Glimepiride
Metformin Hydrochloride
(as Sustained Release)
Excipients
Approved colour used. |
IP
IP |
2mg
500mg
q.s. |
510 |
Metformin Hydrochloride (Sustained Release) , Gliclazide (Sustained Release) & Pioglitazone Tablets |
Each uncoated Bilayered Tablet Contains:
Metformin Hydrochloride
(as Sustained Release)
Gliclazide
(as Sustained Release)
Pioglitazone Hydrochloride
Equ. to Pioglitazone
Excipients
Approved colour used. |
IP
IP
IP |
500mg
30mg
15mg
q.s. |
511 |
Metformin Hydrochloride (Sustained Release) & Glimepiride Tablets IP |
Each Uncoated Bilayered Tablet Contains:
Glimepiride
Metformin Hydrochloride
(as Sustained Release)
Excipients
Approved colour used. |
IP
IP |
1mg
500mg
q.s. |
512 |
Metformin Hydrochloride & GliclazideTablets |
Each uncoated tablets contains:
Metformin hydrochloride
Gliclazide
Excipients
Approved colour used |
IP
IP |
500 mg
80 mg |
513 |
Metformin Hydrochloride Prolonged Release & Glimepiride Tablets IP |
Each uncoated Bilayered tablet contains :
Metformin Hydrochloride
(as Prolonged Release)
Glimepiride
Excipients
Approved colour used |
IP
IP |
1000mg
2mg
q.s |
514 |
Metformin Hydrochloride Sustained-Release Tablets |
Each uncoated Sustained Release Tablet Contains :
Metformin Hydrochloride
Excipients |
IP |
500mg
q.s. |
515 |
Metformin Hydrochloride Sustained-Release Tablets |
Each uncoated Sustained Release Tablet Contains :
Metformin Hydrochloride
Excipients |
IP |
850mg
q.s. |
516 |
Metformin Hydrochloride Sustained-Release Tablets |
Each uncoated Sustained Release Tablet Contains :
Metformin Hydrochloride
Excipients |
IP |
1000mg
q.s. |
517 |
Metformin Hydrochloride Tablets IP |
Each uncoated sustainedrelease tablet contains:
Metformin Hydrochloride
Excipients
Approved colour used |
IP |
500 mg
q.s. |
518 |
Metformin hydrochloride,(ER) Pioglitazone and GlimepirideTablets |
Each uncoated Bilayered tablets contain:
Metformin hydrochloride
(as Extended release)
Pioglitazone Hydrochloride
Eq.to Pioglitazone
Glimepiride
Excipients
Approved colour used |
IP
IP
IP |
500 mg
15 mg
2 mg
q.s |
519 |
Metformin hydrochloride,(ER) Pioglitazone and Glimipride Tablets |
Each uncoated Bilayered tablets contain:
Metformin hydrochloride
(as Extended release)
Pioglitazone Hydrochloride.
Eq.to Pioglitazone
Glimepiride
Excipients
Approved colour used |
IP
IP
IP |
500 mg
15 mg
1 mg
q.s |
520 |
Methotrexate Tablets IP |
Each uncoated tablet contains:
Methotrexate
Excipients
Approved colour used. |
IP |
2.5mg
q.s. |
521 |
Methylcobalamin Sublingual Tablets |
Each uncoated sublingual tablet contains :
Methylcobalamin
Excipients |
IP |
1500mcg
q.s. |
522 |
Methylcobalamin Tablets |
Each film coated Tablet Contains:
Methylcobalamin
Excipients
Approved colour used. |
|
1500mcg
q.s. |
523 |
Methylcobalamin, Alpha Lipoic Acid, Inositol, Folic acid, Chromium Polynicotinate, Selenium Dioxide and Benfotiamine Capsules |
Each hard gelatin Capsules contains:
Methylcobalamin
Alpha LipoicAcid
Inositol
Folic Acid
Chromium Polynicotinate
Selenium Dioxide
Benfotiamine
Excipients
Approved colour Used |
IP
USP
BP
IP |
1500mcg
100mg
100mg
1.5mg
200mcg
55mcg
150mg
q.s |
524 |
Methylcobalamin, Alpha Lipoic Acid, Pyridoxine Hydrochloride,Thia mine Mononitrate & Folic Acid Tablets |
Each film coated tablet contains:
Methylcobalamin
Alpha Lipoic Acid
Pyridoxine Hydrochloride
Thiamine Mononitrate
Folic Acid
Excipients
Approved colour used |
IP
USP
IP
IP
IP |
1500mcg
100mg
3mg
10mg
1.5mg
q.s. |
525 |
Methylcobalamin, Calcium Citrate, Calcitriol, Folic Acid & Pyridoxine Hydrochloride Tablets |
Each film coated Tablet Contains:
Methylcobalamin
Calcium Citrate
Calcitriol
Folic Acid
Pyridoxine Hydrochloride
Excipients
Approved colour used |
IP
USP
IP
IP
IP |
1500mcg
750mg
0.25mcg
1.5mg
3mg
q.s. |
526 |
Methylcobalamin, L-Methylfolate & Pyridoxine HCl Tablets |
Each film coated Tablet Contains :
Methylcobalamin
L-Methylfolate
Pyridoxine HCl
Excipients
Approved Colour Used |
IP
IP |
1500mcg
1MG
0.5mg
q.s |
527 |
Methylcobalamin, L-Methylfolate, Pyridoxal-Phosphate, Vitamin D3 & Docosahexaenoic Acid (DHA) Tablets |
Each film coated tablet contains:
Methylcobalamin
L-Methylfolate
Pyridoxal Phosphate
Vitamin D3
Docosahexaenoic Acid (DHA)
Excipients
Approved colour used.
Appropriate overages of vitamins added to compensate the
loss on storage. |
I.P.
I.P.
I.P.
I.P. |
1500 mcg
1.0 mg
0.5 mg
1000 IU
100 mg
q.s. |
528 |
Methylcobalamine, Alpha Lipoic Acid Vitamin D3,Pyridoxine Hydrochloride ,FolicAcid Tablets |
Each film coatedTablet Contains:
Methylcobalamine
Alpha LipoicAcid
Vitamin D3
Pyridoxine Hydrochloride
Folic Acid
Excipients
Approved Colour Used. |
IP
USP
IP
IP
IP |
1500mcg
100mg
1000IU
3mg
1.5mg
q.s. |
529 |
Methylcobalamine, Alpha Lipoic Acid, Pyridoxine Hydrochloride, Thiamine & Folic Acid Capsules |
Each hard gelatin capsule contains:- Methylcobalamin Alpha Lipoic Acid Pyridoxine Hydrochloride Thiamine Mononitrate Folic Acid Excipients Approved colour used in emptycapsule shells. |
IP USP IP IP IP |
1500 mcg. 100 mg. 3 mg. 10 mg. 1.5 mg. q.s. |
530 |
Methylprednisolone Tablets |
Each uncoated tablet contains:-
Methylprednisolone
Excipients
Colour :- Approved Colour Used |
IP |
8 mg
q.s. |
531 |
Methylprednisolone Tablets IP |
Each uncoated tablet contains:-
Methylprednisolone
Excipients
Colour :- Approved Colour Used |
IP |
4 mg
q.s. |
532 |
Methylprednisolone Tablets IP |
Each uncoated tablet contains:-
Methylprednisolone
Excipients
Colour :- Approved Colour Used |
IP |
2 mg
q.s. |
533 |
Methylprednisolone Tablets IP |
Each uncoated tablet contains:-
Methylprednisolone
Excipients
Colour :- Approved Colour Used |
IP |
16 mg
q.s. |
534 |
Methylprednisolone Tablets IP |
Each uncoated tablet contains:-
Methylprednisolone
Excipients
Colour :- Approved Colour Used |
IP |
16 mg
q.s. |
535 |
Metoprolol Succinate (ER) & Hydrochlorothiazid e Tablets |
Each uncoated Bilayered tablet contains:
Metoprolol Succinate
Eq. to Metoprolol Tartrate
(As Extended Release)
Hydrochlorothiazide
Excipients
Approved colour used |
IP
IP |
47.5 mg
50 mg
12.5 mg
q.s. |
536 |
Metoprolol Succinate (ER) & Hydrochlorothiazid e Tablets |
Each uncoated Bilayered tablet contains:
Metoprolol Succinate
Eq. to Metoprolol Tartrate
(As Extended Release)
Hydrochlorothiazide
Excipients
Approved colour used |
IP
IP |
23.75 mg
25 mg
12.5 mg
q.s. |
537 |
Metoprolol Succinate (ER) Tablets IP |
Each film coated tablet contains:
Metoprolol Succinate
Eq. to Metoprolol Tartrate
(As Extended Release)
Excipients
Approved colour used |
IP |
47.5 mg
50 mg
q.s. |
538 |
Metoprolol Succinate Prolonged release Tablets IP |
Each film coated ProlongedreleaseTablet Contains
Metoprolol succinate
Equ. toMetoprolol Tartrate
Excipients
Colour :-Approved colour used |
IP |
23.75mg
25mg
q.s |
539 |
Metoprolol Succinate(ER) & Amlodipine Besilate Tablets |
Each film coated Bilayered tablet contains:
Metoprolol Succinate
Eq. to Metoprolol Tartrate
(As Extended Release)
Amlodipine Besilate
Eq. to Amlodipine
Excipients
Approved colour used |
IP
IP |
47.5 mg
50 mg
5 mg
q.s. |
540 |
Metoprolol Succinate(ER) & Amlodipine Besilate Tablets |
Each film coated Bilayered tablet contains:
Metoprolol Succinate
Eq. to Metoprolol Tartrate
(As Extended Release)
Amlodipine Besilate
Eq. to Amlodipine
Excipients
Approved colour used |
IP
IP |
23.75 mg
25 mg
5 mg
q.s. |
541 |
Metoprolol SuccinateExtended release Tablets IP |
Each film coated Extended release Tablet Contains
Metoprolol succinate
Equ. ToMetoprolol
TartrateExcipients
Colour:-Approved colour used |
IP |
11.875mg
12.5mg
q.s. |
542 |
Metronidazole and Povidone –Iodine Ointment |
Composition :
Metronidazole
Povidone–Iodine
(Available Iodine 1.0%w/w)
Water Soluble Ointment Base |
IP
IP |
2.0%w/w
10.0%w/w
q.s |
543 |
Metronidazole Oral solution |
Each 5ml contains :
Metronidazole Benzoate
Equ. to Metronidazole
In a flavoured Syrupy Base.
Colour : Approved Coloured Used |
IP |
250mg
q.s |
544 |
Metronidazole Tablet IP |
Each film coated Tablet Contains:
Metronidazole
Excipients
Colour : Approved Coloured Used |
IP |
200mg
q.s |
545 |
Metronidazole Tablet IP |
Each film coated Tablet Contains:
Metronidazole
Excipients
Colour : Approved Coloured Used |
IP |
400mg
q.s |
546 |
Miconazole Nitrate Topical Powder USP |
Composition :
Miconazole Nitrate
Talc |
IP
IP |
2%w/w
q.s |
547 |
Milk of Magnesia, Liquid Paraffin & Sodium Picosulphate Suspension |
Each 5 ml contain:
Milk of Magnesia
Liquid Paraffin
Sodium Picosulphate
Excipients
In a Flavoured Sorbitol base
Approved colour used |
IP
IP
BP |
3.75ml
1.25ml
3.33 mg
q.s. |
548 |
Milk of Magnesia, Liquid Paraffin and Sodium Picosulfate Suspension |
Each 5ml contains:
Liquid Paraffin
Milk of Magnesia
Sodium Picosulphate
Flavoured Non SyrupyBase
Approved colour used |
IP
IP
BP |
1.25ml
3.75ml
3.33mg
q.s. |
549 |
Minocycline Hydrochloride Tablet |
Each film coated Tablet Contains
Minocycline Hydrochloride
Equ. to Minocycline
Excipients
Colour : Approved Coloured Used |
USP |
100mg
q.s |
550 |
Minoxidil Tablets IP |
Each uncoated tablet Contains:
Minoxidil
Excipients
Approved colour used |
IP |
2.5mg
q.s. |
551 |
Minoxidil Tablets IP |
Each Uncoated Tablet Contains:
Minoxidil
Excipients |
IP |
5mg
q.s. |
552 |
Minoxidil Topical solution USP |
Each ml contains:
Minoxidil
Excipients
Approved colour used |
IP |
20mg
q.s |
553 |
Mometasone & Fusidic Acid Cream |
Composition:-
Mometasone furoate
Fusidic Acid
Cream Base |
IP
IP |
0.10%w/w
2.00%w/w
q.s. |
554 |
Mometasone Furoate & Terbinafine Hydrochloride Cream |
Mometasone Furoate
Terbinafine Hydrochloride
Cream Base |
IP
IP |
0.1% w/w
1% w/w
q.s. |
555 |
Mometasone Furoate& Salicylic Acid Lotion |
Composition :
Mometasone Furoate
Salicylic Acid
In an Emollient Base Containing Hexylene Glycol
Preservatives :
Methylparaben
Propylparaben |
IP
IP
IP
IP |
0.10%w/w
3.50%w/w
0.20%w/w
0.02%w/w |
556 |
Mometasone FuroateCream IP |
Composition :
Mometasone Furoate
Cream Base |
IP |
0.1% w/w
q.s. |
557 |
Mometasone FuroateOintment |
Each g contains
Mometasone Furoate
Excipients |
IP |
0.1% w/w
q.s. |
558 |
Mometasone, Hydroquinone and Tretinoine Cream |
Composition
Mometasone furoate
Hydroquinone
Tretinoine
Excipients |
IP
USP
USP |
0.1 % w/w
2 % w/w
0.025 %w/w
q.s. |
559 |
Montelukast & Doxophylline (SR) Tablets |
Each uncoated tablet contains:-
Montelukast Sodium
Equivalent to Montelukast
Doxophylline
(AsSustained Release)
Excipients
Colour:-Approved colour used |
IP
IP |
10 mg
400 mg
q.s |
560 |
Montelukast & Levocetirizine HCL Dispersible Tablets |
Each uncoated dispersible tablet contains:
Montelukast sodium
Eq.to Montelukast
Levocetirizine HCL
Excipients
Approved colour used |
IP
IP |
4 mg
2.5 mg |
561 |
Montelukast & Levocetirizine HCl Tablets |
Each uncoated Bilayered Tablet Contains :
Montelukast Sodium
Equ. to Montelukast
Levocetirizine Hydrochloride
Excipients
Approved colour used. |
IP
IP |
10mg
5mg
q.s. |
562 |
Montelukast sodium & Bambuterol Hydrochloride Tablets |
Each film coated Tablet contains:
Montelukast sodium
Equ. to Montelukast
Bambuterol Hydrochloride
Excipients
Approved colour used |
IP
BP |
10mg
10mg
q.s. |
563 |
Montelukast Sodium & Desloratadine Tablet |
Each film coated Tablet Contains:-
Montelukast Sodium
Equivalent toMontelukast
Desloratadine
Excipients
Approved colour used |
IP
BP |
10 mg
5 mg
q.s |
564 |
Montelukast Sodium & Levocetirizine Dihydrochloride DispersibleTablets |
Each Uncoated DispersibleTablet Contains:
Montelukast Sodium
Equ. To Montelukast
LevocetirizineDihydrochloride
Excipients
Colour : Approved Coloured used |
IP
IP |
5mg
2.5mg
q.s. |
565 |
Montelukast Sodium & Levocetirizine Dihydrochloride Tablets IP |
Each uncoated Tablet contains:
Montelukast sodium
Equ. to Montelukast
LevocetirizineDihydrochloride
Excipients
Approved colour used. |
IP
IP |
10mg
5mg
q.s |
566 |
Montelukast Sodium & Levocetirizine Dihydrochloride Tablets IP |
Each UncoatedTablet Contains:-
Montelukast Sodium
eq. to Montelukast
LevocetirizineDihydrochloride
Excipients
Approved colour used |
IP
IP |
4mg
2.5mg
q.s. |
567 |
Montelukast Sodium & Levocetirizine Hydrochloride Tablets IP |
Each Uncoated Tablet Contains:-
Montelukast Sodium
eq. to Montelukast
Levocetirizine Hydrochloride
Excipients
Approved colour used |
IP
IP |
4mg
2.5mg
q.s. |
568 |
Montelukast Sodium & Levocetirizine Hydrochloride Tablets IP |
Each film coated Tablet Contains:-
Montelukast Sodium
eq. to Montelukast
Levocetirizine Hydrochloride
Excipients
Approved colour used |
IP
IP |
10 mg
5mg
q.s |
569 |
Montelukast Sodium Chewable Tablets |
Each UncoatedChewableTablet Contains:
Montelukast sodium
Equ. To
Montelukast
Excipients |
IP |
4mg
q.s. |
570 |
Montelukast Sodium Tablets IP |
Each Film coated Tablet Contains :
Montelukast Sodium
Equ. to Montelukast
Excipients
Approved colour used |
IP |
10mg
q.s. |
571 |
Montelukast Sodium, Fexofenadine Hydrochloride and Sustained Release Acebrophylline Tablets |
Each film coated Tablet contains:
Montelukast sodium
Equ. to Montelukast
Fexofenadine Hydrochloride
Acebrophylline
(As sustainedrelease form)
Excipients
Approved colour used |
IP
IP |
10mg
120mg
200mg
q.s |
572 |
Montelukast sodium, Levoceterizine dihydrochloride & Ambroxol hydrochloride Tablets |
Each filmcoated tablets contains:
Montelukast sodium
Equivalent to Montelukast
Levoceterizine dihydrochloride
Ambroxol hydrochloride
(As sustainedrelease)
Excipients
Approved colour used |
IP
IP
IP |
10 mg
5 mg
75 mg
q.s. |
573 |
Moxifloxacin Hydrochloride Tablets |
Each Film coated Tablet Contains:
Moxifloxacin Hydrochloride
Equ. To
Moxifloxacin
Excipients
Approved colour used. |
IP |
400mg
q.s |
574 |
Moxonidine Tablets |
Each film coated tablet contains:
Moxonidine
Excipients
Approved colour used |
BP |
0.2mg
q.s. |
575 |
Moxonidine Tablets |
Each film coated tablet contains:
Moxonidine
Excipients
Approved colour used |
BP |
0.3mg
q.s. |
576 |
Multivitamin , Multimineral with LycopeneCapsules |
Each hard gelatin capsule contains
Lycopene 6%
Lutien 8%
Beta Carotene (10% Dispersion)
Vitamin B6
Vitamin B12
Vitamin D3
Folic Acid
Calcium Pantothenate
Niacinamide
Biotin
Lysine Hydrochloride
Ferrous Fumarate
Dibasic Calcium Phosphate
Zinc Sulphate
Magnesium Hydroxide
Copper Sulphate
Manganese Sulphate
Chromium Chloride
Sodium Selenate
Excipients
Approved colour used in emptycapsule shells. |
USP
USP
USP
IP
IP
IP
IP
IP
IP
USP
USP
IP
IP
IP
IP
USP
USP
USP |
5mg
6mg
10mg
1mg
5mcg
200IU
500mcg
5mg
25mg
10mcg
50mg
45mg
75mg
10mg
10mg
500mcg
500mcg
200mcg
100mcg
q.s |
577 |
Multivitamin Multimineral & Antioxidant suspension |
Each 5ml contains:
Cholecalciferol (as Stabilized)
Pyridoxine HCL
Niacinamide
Cyanocobalamin
Zinc (as Zinc Gluconate )
B-Carotene Dispersion 2.5%
Manganese
(as Manganese Chloride Tetrahydrate)
Molybdenum
(as Sodium Molybdate Dihydrate )
Selenium (as Sodium Selenate)
Lysine Hydrochloride
Iodine(as Potassium Iodide )
Biotin
Chromiume
(as Chromium Chloride Hexahydrate)
Inositol
Excipients
In a flavoured syrupy base
Approved colour used. |
IP
IP
IP
IP
USP
USP
BP
BP
IP
USP
USP
USP |
200IU
1mg
15mg
1mcg
3mg
38mg
0.8mg
8mcg
10mcg
30mg
50mcg
10mcg
10mcg
10mg
q.s. |
578 |
Multivitamin, Iron, folic acid & Lysine Drops |
Each ml contains:
Vitamin A(as Palmitate)
Vitamin D3
Ferric Ammonium citrate
(eq.to Element iron)
Vitamin B12
Folic acid
Lysine Monohydrochloride
Thiamine Hydrochloride
Vitamin B2
Vitamin B6
D-Panthenol
Niacinamide
Flavoured syrupy base
Approved Colour Used |
IP
IP
IP
IP
IP
USP
IP
IP
IP
IP
IP |
5000IU
400IU
25mg
5mcg
0.2mg
100mg
1mg
1mg
1mg
3mg
10mg
q.s |
579 |
Mupirocin ointment IP |
Composition :-
Mupirocin Topical
Ointment Base |
IP |
2.0%w/w
q.s. |
580 |
Naproxen & Domperidone Tablets |
Each Film coatedtablet contains:
Naproxen
Domperidone
Excipients
Approved colour used. |
IP
IP |
250 mg
10 mg
q.s |
581 |
Naproxen & Domperidone Tablets |
Each film coated tablet contains:
Naproxen
Domperidone
Excipients
Approved colour used |
IP
IP |
500mg
10mg
q.s |
582 |
Naproxen Sodium & Domperidone Tablet |
Each uncoated tablet contain:
Naproxen Sodium
Domperidone
Excipients
Approved colour used |
IP
IP |
250 mg
10 mg
q.s |
583 |
Naproxen Sustained Release Tablets IP |
Each uncoated sustained release tablet contains:
Naproxen
Excipients
Approved colour used |
IP |
750mg
q.s. |
584 |
Naproxen Tablet IP |
Each uncoated tablet contain:
Naproxen
Excipients
Approved colour used |
IP |
250 mg
q.s |
585 |
Naproxen Tablet IP |
Each uncoated tablet contain:
Naproxen
Excipients
Approved colour used |
IP |
500 mg
q.s |
586 |
Nebivolol & Hydrochlorothiazid e Tablets |
Each uncoated Tablets Contains:
Nebivolol Hydrochloride
Equ. to Nebivolol
Hydrochlorothiazide
Excipients
Approved colour used. |
IP
IP |
5mg
12.5mg
q.s. |
587 |
Nebivolol Hydrochloride Tablets IP |
Each uncoated tablet contains:
Nebivolol Hydrochloride
Eq. to Nebivolol
Excipients
Approved colour used. |
IP |
5mg
q.s. |
588 |
Neomycin and Polymyxin B Sulfate and Bacitracin Zinc Ointment USP |
Composition :
Each gm Contains :
Polymyxin B Sulfate
Equ. to Polymyxin
Bacitracin Zinc
Equ. to Bacitracin
Neomycin Sulphate
Equ. to Neomycin
Preservative:
Benzyl Alcohol
Ointment Base |
USP
IP
IP
IP |
5000 units
400units
3400units
0.1%w/w
q.s |
589 |
Neomycin, Miconazole Nitrate & Fluocinolone Acetonide Cream |
Composition :
Miconazole Nitrate
Neomycin Sulphate
Equ. to Neomycin
Fluocinolone Acetonide
Preservatives:
Chlorocresol
Cream Base |
IP
IP
IP
IP |
2.0%w/w
0.5%w/w
0.01%w/w
0.1%w/w
q.s |
590 |
Nicorandil Tablets IP |
Each uncoated Tablets Contains:
Nicorandil
Excipients |
IP |
5mg |
591 |
Nicorandil Tablets IP |
Each uncoated Tablets Contains:
Nicorandil
Excipients |
IP |
10mg |
592 |
Nifedipine Prolonged Release Tablets BP |
Each Prolonged Release film coated tablet contains:
Nifedipine
Excipients
Approved colour used. |
BP |
30mg
q.s. |
593 |
Nimesulide & Paracetamol Tablets |
Each uncoated tablet contains:
Nimesulide
Paracetamol
Excipients |
BP
IP |
20 mg
q.s. |
594 |
Nimesulide & Paracetamol Tablets |
Each uncoated Bilayered Tablet contains:
Nimesulide
Paracetamol
Excipients
Approved colour used. |
BP
IP |
100mg
325mg
q.s. |
595 |
Nimesulide Mouth Dissolving Tablets |
Each uncoated Mouth dissolving Tablet contains :
Nimesulide
Excipients
Approved colour used. |
BP |
100mg
q.s. |
596 |
Nimesulide Tablets |
Each uncoated tablet contains:-
Nimesulide
Excipients
Colour:-Approved colour used |
BP |
100 mg
q.s |
597 |
Nimesulide, Paracetamol & Chlorzoxazone Tablets |
Each film coated tablet contains:
Nimesulide
Paracetamol
Chlorzoxazone
Excipients
Approved colour used |
BP
IP
USP |
100mg
325mg
250mg
q.s |
598 |
Nimesulide, Paracetamol, Phenylephrine HCl & Caffeine Tablets |
Each uncoated Tablet Contains:
Nimesulide
Paracetamol
Phenylephrine Hydrochloride
Caffeine (anhydrous)
Excipients |
BP
IP
IP
IP |
100mg
325mg
10mg
25mg
q.s. |
599 |
Nimesulide, Paracetamol, Serratiopeptidase Tablets |
Each film coated tablet contains :
Nimesulide
Paracetamol
Serratiopeptidase
((Eq. to enzyme activityof 30000 units of enteric coated
granules)
Excipients
Approved colour used. |
BP
IP
IP |
100mg
325mg
15mg |
600 |
Nimesulide, Phenylephrine HCL, Cetirizine Dihydrochloride & Caffeine Tablets |
Each uncoated tablet contains:-
Nimesulide
Phenylephrine Hydrochloride
Cetirizine Dihydrochloride
Caffeine (anhydrous)
Excipients
Colour:-Approved colour used |
BP
IP
IP
IP |
100 mg
10 mg
5 mg
30 mg
q.s. |
601 |
Nimesulide, Phenylephrine HCl& Levocetirizine HCl Tablets |
Each uncoated tablet contains:
Nimesulide
Phenylephrine HCl
Levocetirizine HCl
Excipients
Approved Colour used |
BP
IP
IP |
100mg
5mg
5mg
q.s. |
602 |
Nimesulide, Phenylephrine Hydrochloride, Cetirizine Dihydrochloride & Caffeine Tablets |
Each film Coated Tablet Contains :
Nimesulide
Phenylephrine Hydrochloride
Cetirizine Dihydrochloride
Caffeine ( Anhydrous)
Excipients
Approved colour Used. |
BP
IP
IP
IP |
100mg
10mg
5mg
30mg
q.s. |
603 |
Nimodipine Tablets |
Each Film coated Tablet Contains :
Nimodipine
Excipients
Approved colour used. |
IP |
30mg
q.s. |
604 |
Nitazoxanide for Oral Suspension |
Composition :
Each 5ml of reconstituted suspension contains
Nitazoxanide
Excipients
Approved Colour used |
|
100mg
q.s |
605 |
Nitrofurantoin SR Tablet |
Each FilmCoated Sustained ReleaseTablet Contains
Nitrofurantoin
Excipients
Colour :-Approved colour used |
BP |
100mg
q.s. |
606 |
Nitroglycerine Controlled Release Tablet |
Each uncoated Tablet contains:
Diluted Nitroglycerine
Equ. to Nitroglycerin
(as Controlled Release)
Excipients
Approved colour used |
IP |
2.6mg
q.s. |
607 |
Norfloxacin & TinidazoleTablets |
Each film coated tablet contains:-
Norfloxacin
Tinidazole
Excipients
Colour:-Approved colour used |
IP
IP |
400 mg
600 mg
q.s. |
608 |
Norfloxacin Tablets IP |
Each film coated Tablet Contains:
Norfloxacin
Excipients
Approved Colour Use |
IP |
400mg
q.s |
609 |
Nortriptyline & Gabapentin Tablets |
Each Film coated Tablet Contains:-
Nortriptyline Hydrochloride
Equivalent to Nortriptyline
Gabapentin
Excipients
Approved colour used |
IP
IP |
10 mg
400 mg
q.s. |
610 |
Nortriptyline & PregabalineTablets |
Each film coatedTablet Contains:
Nortriptyline Hydrochloride
Equivalent to Nortriptyline
Pregabaline
Excipients
Approved colour used |
IP
IP |
10 mg
75 mg
q.s. |
611 |
Nortriptyline, Pregabalin (SR) & Methylcobalamin Tablets |
Each film coated Bilayered Tablet Contains:
Nortriptyline Hydrochloride
Equivalent to Nortriptyline
Pregabalin
(as Sustained Release)
Methylcobalamin
Excipient
Approved colour used |
IP
IP
IP |
10 mg
75 mg
1500mcg
q.s. |
612 |
Nortriptyline, Pregabalin & Mecobalamin Tablets |
Each film coatedTablet Contains:
Nortriptyline Hydrochloride
Equivalent to Nortriptyline
Pregabalin
Mecobalamin
Excipient
Approved colour used |
IP
IP
IP |
10 mg
75 mg
1500mcg
q.s. |
613 |
Nortriptyline, Pregabalin & Methylcobalamin Tablets |
Each film coated Bilayered Tablet Contains:
Nortriptyline Hydrochloride
Equivalent to Nortriptyline
Pregabalin
Methylcobalamin
Excipient
Approved colour used |
IP
IP
IP |
10 mg
75 mg
1500mcg
q.s. |
614 |
Ofloxacin & Lactic Acid Bacillus Tablets |
Each Film coated Tablet Contains :
Ofloxacin
Lactic Acid Bacillus
Excipients
Approved colour used. |
IP |
200mg
60 Million
Spores
q.s. |
615 |
Ofloxacin & Metronidazole Suspension |
Each 5ml contains :
Ofloxacin
Metronidazole Benzoate
Equ. to Metronidazole
In a Flavoured SyrupyBase
Colour : Sunset Yellow FCF |
IP
IP |
50mg
100mg
q.s |
616 |
Ofloxacin & Metronidazole Suspension |
Each 5ml contains :
Ofloxacin
Metronidazole Benzoate
Equ. to Metronidazole
Flavoured Syrupy base
Approved colour used. |
IP
IP |
50mg
120mg
q.s |
617 |
Ofloxacin & Metronidazole Suspension |
Each 5ml contains :
Ofloxacin
Metronidazole Benzoate
Equ. To Metronidazole
In a Flavoured Palatable Base
Colour: - Approved colour used. |
IP
IP |
100mg
200mg
q.s. |
618 |
Ofloxacin & Ornidazole Tablet IP |
Each FilmCoatedTabletContains:
Ofloxacin
Ornidazole
Excipients
Approved colour used |
IP
IP
q.s. |
200 mg
500 mg |
619 |
Ofloxacin & TinidazoleTablets |
Each film coated tablet contains:
Ofloxacin
Tinidazole
Excipients
Approved colour used. |
IP
IP |
200mg
600mg
q.s. |
620 |
Ofloxacin Oral Suspension IP |
Each 5 ml contains:
Ofloxacin
Excipients
Approved colour used |
IP |
50 mg |
621 |
Ofloxacin oral suspension IP |
Each 5ml ofsuspension contains
Ofloxacin
In a flavoured Syrupybase.
Approved Colour Used. |
IP |
100mg
q.s. |
622 |
Ofloxacin Tablet IP |
Each film coated tablet contains:-
Ofloxacin
Excipients
Approved colour used |
IP |
400 mg
q.s. |
623 |
Ofloxacin Tablets IP |
Each film coated tablet contains:-
Ofloxacin
Excipients
Colour:-Approved colour used |
IP |
200 mg
q.s. |
624 |
Ofloxacin, Flucinolone Acetonide, Clotrimazole & Chlorocresol Cream |
Composition :
Ofloxacin
Flucinolone Acetonide
Clotrimazole
Chlorocresol
(as Preservative)
Cream Base |
IP
IP
IP
IP |
0.5%w/w
0.01%w/w
1%w/w
0.1%w/w
q.s. |
625 |
Ofloxacin, Metronidazole Benzoate & Simethicone Suspension |
Each 5ml Contains:-
Ofloxacin
MetronidazoleBenzoate
Equivalent toMetronidazole
Simethicone
In flavoured Syrupybase
Approved colour used |
IP
IP
IP |
50 mg
120mg
10 mg
q.s. |
626 |
Ofloxacin, Ornidazole, Itraconazole and Clobetasole PropionateCream |
Composition
Ofloxacin
Ornidazole
Itraconazole
Clobetasole Propionate
Methyl Paraben (Preservative)
Propyl Paraben (Preservative)
In cream base |
IP
IP
USP
IP
IP
IP |
0.75 % w/w
2.0 % w/w
1 % w/w
0.05 % w/w
0.20% w/w
0.02% w/w
q.s. |
627 |
OlanzapineTablet IP |
Each film coated tablet contains:
Olanzapine
Excipients
Approved colour used |
IP |
5mg
q.s. |
628 |
OlanzapineTablet IP |
Each film coated tablet contains:
Olanzapine
Excipients
Approved colour used |
IP |
2.5mg
q.s. |
629 |
OlanzapineTablet IP |
Each film coated tablet contains:
Olanzapine
Excipients
Approved colour used |
IP |
7.5 mg
q.s. |
630 |
OlanzapineTablets IP |
Each film coated tablet contains:
Olanzapine
Excipients
Approved colour used |
IP |
10 mg
q.s. |
631 |
Olmesartan & AmlodipineTablets |
|
IP
IP |
20 mg
5 mg
q.s |
632 |
Olmesartan & Chlorthalidone Tablets |
Each film coated tablet contains:
Olmesartan Medoxomil
Chlorthalidone
Excipients
Approved colour used |
IP
IP |
20 mg
12.5 mg
q.s |
633 |
Olmesartan & Hydrochlorothiazid e Tablets |
Each film coated tablet contains:
Olmesartan Medoxomil
Hydrochlorothiazide
Excipients
Approved colour used |
IP
IP |
20 mg
12.5 mg
q.s |
634 |
Olmesartan & Metoprolol SuccinateTablets |
Each film coated Bilayered tablet contains:
Olmesartan Medoxomil
Metoprolol Succinate
Eq. to Metoprolol Tartrate
(As Extended Release)
Excipients
Approved colour used |
IP
IP |
20 mg
47.5 mg
50 mg
q.s |
635 |
Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazid e Tablets |
Each film coated Tablet Contains:
Olmesartan Medoxomil
AmlodipineBesylate
Equ. To Amlodipine
Hydrochlorothiazide
Excipients
ApprovedColour used. |
IP
IP
IP |
40mg
5mg
12.5mg
q.s. |
636 |
Olmesartan, Amlodipine & Hydrochlorothiazid e Tablets |
Each film coated tablet contains:
Olmesartan Medoxomil
Amlodipine Besilate
Eq. to Amlodipine
Hydrochlorothiazide
Excipients
Approved colour used |
IP
IP
IP |
20 mg
5 mg
12.5 mg
q.s |
637 |
Olmesarton Medoxomil & Hydrochlorthiazide Tablet |
Each film coated tablet contains:
Olmesarton Medoxomil
Hydrochlorthiazide
Excipients
Approved colour used |
IP
IP |
40 mg
12.5 mg
q.s. |
638 |
Olmesarton Medoxomil Tablet IP |
Each film coated tablet contains:
Olmesarton Medoxomil
Excipients
Approved colour used |
IP |
20 mg
q.s. |
639 |
Olmesarton Medoxomil Tablet IP |
Each film coated tablet contains:
Olmesarton Medoxomil
Excipients
Approved colour used |
IP |
40 mg
q.s. |
640 |
Omeprazole (Delayed- Release) and Domperidone (Sustained-Release) Capsules |
Each capsule contains:
Omeprazole
(as enteric coated pellets)
Domperidone
(as sustained Release pellets)
Colour : Titanium Dioxide
Approved colour used in emptycapsule shel |
IP
IP |
20mg
30mg |
641 |
Omeprazole (EntericCoated) & Domperidone Capsules IP |
Each hard gelatin capsule contains:-
Omeprazole
(As Enteric Coated Pellets)
Domperidone
Excipients
Approved colour used in emptycapsule shells. |
IP
IP |
20 mg
10 mg
q.s |
642 |
Omeprazole Capsule IP |
Each hard gelatin capsule contains:-
Omeprazole
(As enteric coated pellets)
Excipients
Approved colour used in emptycapsule shells. |
IP |
20mg.
q.s. |
643 |
Ondansetron Oral Solution IP |
Each 5 ml contains:
Ondansetron Hydrochloride
Equ.to ondansetron
Flavoured syrupybase |
IP
q.s |
2 mg
q.s. |
644 |
Ondansetron Oral Solution IP |
Each 5 ml contains:
Ondansetron Hydrochloride
Equ. to Ondansetron
Flavoured Syrupy Base |
IP |
4mg
q.s. |
645 |
Ondansetron Orally Disintegrating TabletsTablet IP |
Each Uncoated OrallyDisintegrating Tablets Contains
Ondansetron hydrochloride
Equ. toOndansetron
Excipients
Approved colour used. |
IP |
4mg |
646 |
Ondansetron Orally Disintegrating TabletsTablet IP |
Each Uncoated OrallyDisintegrating Tablets Contains
Ondansetron hydrochloride
Equ. toOndansetron
Excipients
Approved colour used |
IP |
8mg |
647 |
Oral Rehydrat ion Salts IP |
Each Pack contains:
Sodium Chloride
Potassium Chloride
Sodium Citrate
Dextrose Anhydrous
Excipients |
IP
IP
IP
IP |
0.52g
0.30g
0.58g
2.70g
q.s. |
648 |
Oral Rehydration Salt IP |
Composition:
Each sachet(21.8gm) contains:
Dextrose (Anhydrous)
Potassium Chloride
Sodium Chloride
Sodium Citrate
Excipients |
IP
IP
IP
IP |
13.5gm
1.5gm
2.6gm
2.9gm
q.s |
649 |
Orlistat Capsules USP |
Each Hard Gelatin Capsules Contains:
Orlistat ( as Pellets)
Excipients
Approved colour used in EmptyCapsule Shells |
USP |
120mg
q.s. |
650 |
Ornidazole , Diloxanide & Simethicone Tablets |
Each film coated tablet contains:
Ornidazole
Diloxanide furoate
Simethicone
Excipients
Approved colour used. |
IP
IP
IP |
250mg
375mg
25mg
q.s. |
651 |
Ornidazole Tablets |
Each Film coated Tablet Contains :
Ornidazole
Excipients
Approved colour used. |
IP |
500mg
q.s. |
652 |
Oxaceprol Capsules |
Each Hard Gelatin Capsules Contains:
Oxaceprol
Excipients
Approved colour used in emptyCapsule Shells |
|
200mg
q.s. |
653 |
Pancreatin, Simethicone & Activated Charcoal Tablets |
Each film coated Tablet Contains:
Pancreatin
Simethicone
Activated Charcoal
Excipients
Approved colour used |
IP
IP
IP |
175mg
50mg
50mg
q.s. |
654 |
Pantoprazole Gastro-resistant and Domperidone Prolonged –release Capsules IP |
Each hard gelatin capsule contains:-
Pantoprazole Sodium Sesquihydrate
Equivalent to Pantoprazole
(As Enteric Coated Pellets)
Domperidone
(As Prolonged Release Pellets)
Excipients
Approved colour used in emptycapsule shells. |
IP
IP |
40 mg
30 mg
q.s |
655 |
Pantoprazole Gastro-resistant and Domperidone Prolonged –release Capsules IP |
Each hard gelatin capsule contains:-
Pantoprazole Sodium Sesquihydrate
Equivalent to Pantoprazole
(As Enteric Coated Pellets)
Domperidone
(As Sustained Release Pellets)
Excipients
Approved colour used in emptycapsule shells. |
IP
IP |
40 mg
30 mg
q.s |
656 |
Pantoprazole Gastro-Resistant Tablets IP |
Each enteric coated tablet contains:-
Pantoprazole Sodium
Eq. to Pantoprazole
Excipients
Colour:-Approved colour used |
IP |
40 mg
q.s. |
657 |
Pantoprazole Sodium (Enteric coated) & Domperidone (Sustained Release) Capsules IP |
Each hard gelatin capsule contains:-
Pantoprazole Sodium Sesquihydrate
Equivalent to Pantoprazole
(As Enteric Coated Pellets)
Domperidone
(As Sustained Release Pellets)
Excipients
Approved colour used in emptycapsule shells. |
IP
IP |
40 mg
30 mg
q.s |
658 |
Pantoprazole Sodium (Enteric Coated) &Itopride Hydrochloride (Sustained Release) Capsule |
Each Hard Gelatin Capsule contain:
Pantoprazole Sodium Sesquihydrate
Equivalent to Pantoprazole
(As enteric coated pellets)
Itopride Hydrochloride
(As sustainedrelease pellets)
Excipients
Approved colour used in emptycapsule shells |
IP |
40 mg
150 mg
q.s. |
659 |
Pantoprazole Sodium (Enteric Coated)& Levosulpiride (sustained Release) Capsules |
Each Hard Gelatin Capsule Contains
Pantoprazole Sodium Sesquihydrate
Equivalent to Pantoprazole
(As a EntericCoated Pellets)
Levosulpiride
(As Sustained Release Pellets)
Excipients
Approved colour used in emptycapsule shells |
IP |
40 mg
75 mg
q.s. |
660 |
Pantoprazole Sodium & Domperidone Tablets |
Each enteric coated tablet contains:-
Pantoprazole Sodium
Eq. to Pantoprazole
Domperidone
Excipients
Colour:-Approved colour used |
IP
IP |
40 mg
10 mg
q.s. |
661 |
Pantoprazole Tablets IP |
Each enteric coated Tablet contains :
Pantoprazole sodium sesquihydrate
Equ. to Pantoprazole
Excipients
Approved colour used |
IP |
20mg
q.s. |
662 |
Paracetamol , Phenylephrine HCl & Cetirizine HCl, Tablets |
Each uncoated tablet contains:
Paracetamol
Phenylephrine Hydrochloride
Cetirizine Dihydrochloride
Excipients
Approved colour used.
(Banned Drug 12/08/2024) |
IP
IP
IP |
325mg
5mg
5mg
q.s. |
663 |
Paracetamol , Phenylephrine Hydrochloride &Cetirizine Dihydrochloride suspension |
Each 5ml contains:
Paracetamol
Phenylephrine Hydrochloride
Cetirizine Dihydrochloride
In a flavoured base
Approved colour used
(Banned drug 12/08/2024) |
IP
IP
IP |
250mg
2.5mg
2.5mg
q.s |
664 |
Paracetamol (DT) Tablets BP |
Each uncoated dispersible tablet contains:
Paracetamol
Excipients
Approved colour used. |
IP |
650 mg
q.s. |
665 |
Paracetamol & Diclofenac Tablets IP |
Each uncoated tablet contains:-
Paracetamol
Diclofenac Sodium
Excipients
Colour:-Approved colour used |
IP
IP |
325 mg
50 mg
q.s. |
666 |
Paracetamol & Dicyclomine Hydrochloride Tablets |
Each uncoated Tablet contains:
Paracetamol
Dicyclomine Hydrochloride
Excipients |
IP
IP |
325mg
20mg
q.s. |
667 |
Paracetamol & Domperidone MaleateSuspension |
Each 5ml contains :
Paracetamol
Domperidone Maleate
Flavoured Palatable Base
Colour : Sunset Yellow FCF |
IP
IP |
125mg
5mg
q.s |
668 |
Paracetamol & Domperidone Suspension |
Each 5ml contains:
Paracetamol
Domperidone
In a Flavoured syrupyBase
Approved colour used |
IP
IP |
250mg
5mg
q.s. |
669 |
Paracetamol & Domperidone Tablets |
Each uncoatedtablet contains :
Paracetamol
Domperidone
Excipients
Approved colour used. |
IP
IP |
325mg
10mg
q.s. |
670 |
Paracetamol & Mefenamic Acid Suspension |
Each 5ml Contains
Paracetamol
Mefenamic Acid
In flavoured Palatable base
Approved colour used |
IP
IP |
125mg
50mg
q.s. |
671 |
Paracetamol & Phenylephrine & Chlorpheniramine maleate Suspension |
Each 5 ml contains :-
Paracetamol
Phenylephrine HCl
Chlorpheniramine maleate
In flavoured syrupyBase.
Approved Colour Used. |
IP
IP
IP
IP |
250mg
5mg
2mg
q.s. |
672 |
Paracetamol and CaffeineTablets IP |
Each uncoated Tablet contains:
Paracetamol
Caffeine
Excipients |
IP
IP |
650mg
50mg
q.s. |
673 |
Paracetamol and CaffeineTablets IP |
Each Film Coated Tablet contains:
Paracetamol
Caffeine
Excipients
Approved Colour used. |
IP
IP |
650mg
50mg
q.s. |
674 |
Paracetamol Bilayered Sustained Release Tablets |
Each uncoated Bilayered Sustained Release Tablet contains :
Paracetamol (As Immediate Release)
Paracetamol (As Sustained Release)
Excipients
Approved Colour used. |
IP
IP |
300mg
700mg
q.s. |
675 |
Paracetamol Oral Drops |
Each ml Contains:
Paracetamol
Flavoured Palatable base |
IP |
100mg
q.s |
676 |
Paracetamol Paediatric Oral Suspension IP |
Each 5ml contains:
Paracetamol
In a Flavoured SyrupyBase.
Approved colour used |
IP |
240mg
q.s. |
677 |
Paracetamol Paediatric Oral Suspension IP |
Each 5ml contains:
Paracetamol
In a Flavoured SyrupyBase
Approved colour used |
IP |
120mg
q.s. |
678 |
Paracetamol Suspension IP |
Each 5ml Contains
Paracetamol
Excipients
Approved colour used |
IP |
125mg
q.s. |
679 |
Paracetamol Suspension IP |
Each 5ml Contains
Paracetamol
In flavoured Palatablebase
Approved colour used |
IP |
250mg
q.s. |
680 |
Paracetamol Tablets IP |
Each uncoated tablet contains:-
Paracetamol
Excipients
Colour:-Approved colour used |
IP |
650 mg
q.s. |
681 |
Paracetamol Tablets IP |
Each uncoated tablet contains:-
Paracetamol
Excipients
Approved colour used |
IP |
500 mg
q.s. |
682 |
Paracetamol, Cetirizine Dihydrochloride & Phenylephrine Hydrochloride Tablets |
Each uncoated Tablet contains:
Paracetamol
Cetirizine Hydrochloride
Phenylephrine Hydrochloride
Excipients
Approved colour used
(Banned drug 12/08/2024) |
IP
IP
IP |
500mg
5mg
10mg
q.s |
683 |
Paracetamol, Chlorpheniramine Maleate & Phenylephrine HCl Drops |
Each ml contains
Paracetamol
Chlorpheniramine Maleate
Phenylephrine Hydrochloride
Flavoured Palatable Base
Approved Colour Used |
IP
IP
IP |
125mg
1mg
2.5mg |
684 |
Paracetamol, Chlorpheniramine Maleate & Phenylephrine Hydrochloride Suspension |
Each 5ml contains
Paracetamol
Chlorpheniramine Maleate
Phenylephrine Hydrochloride
Flavoured Palatable Base
Approved Colour Used. |
IP
IP
IP |
125mg
1mg
2.5mg |
685 |
Paracetamol, Dextromethorph nHBr,Cetirizine HCL, ,Phenylephrine HCL, Sodium Citrate & Menthol Suspension |
Each 5ml Contains:
Paracetamol
Dextromethorphan HBr
Cetirizine HCL
Phenylephrine HCL
Sodium Citrate
Menthol
Ina flavoured syrupy base
Approved colour use |
IP
IP
IP
IP
IP
IP |
250mg
5mg
2.5mg
5mg
25mg
1mg
q.s |
686 |
Paracetamol, Phenylephrine HCL & Chlorpheniramine Maleate Tablets |
Each uncoated tablet contains:
Paracetamol
Phenylephrine HCL
Chlorpheniramine Maleate
Excipients
Approved colour used . |
IP
IP
IP |
500mg
10mg
2mg
q.s. |
687 |
Paracetamol, Phenylephrine HCL, & Chlorpheniramine MaleateSuspension |
Each 5ml Contains:-
Paracetamol
Phenylephrine HCL
Chlorpheniramine Maleate
In flavoured Palatablebase
Approved colour used |
IP
IP
IP |
125 mg
5 mg
1 mg
q.s. |
688 |
Paracetamol, Phenylephrine HCl, Cetirizine Tablet |
Each Uncoated Tablet Contains:
Paracetamol
Phenylephrine Hydrochloride
Cetirizine
Excipients
Approved Colour Used
(Banned drug 12/08/2024) |
IP
IP
IP |
325mg
10mg
5mg
q.s |
689 |
Paracetamol, Phenylephrine HCL, Chlorpheniramine Maleate, Sodium Citrate & Menthol Suspension |
Each 5ml Contains:-
Paracetamol
Phenylephrine HCL
Chlorpheniramine Maleate
Sodium Citrate
Menthol
In flavoured Syrupybase
Approved colour used |
IP
IP
IP
IP
IP |
250 mg
5 mg
0.5 mg
60 mg
1 mg
q.s. |
690 |
Paracetamol, Phenylephrine HCL, Chlorpheniramine Maleate, Sodium Citrate & Menthol Suspension |
Each 5ml Contains:-
Paracetamol
Phenylephrine HCL
Chlorpheniramine Maleate
Sodium Citrate
Menthol
In flavoured Syrupybase
Approved colour used |
IP
IP
IP
IP
IP |
125 mg
5 mg
0.5 mg
60 mg
1 mg
q.s. |
691 |
Paracetamol, Phenylephrine HCL,Caffeine , & Chlorpheniramine Maleate Tablets |
Each uncoated tablet contains:
Paracetamol
Phenylephrine Hydrochloride
Caffeine (Anhydrous)
Chlorpheniramine Maleate
Excipients
Approved colour used |
IP
IP
IP
IP |
500 mg
12.5 mg
30mg
2 mg
q.s |
692 |
Paracetamol, Phenylephrine Hydrochloride , Guaiphenesin, Cetirizine Hydrochloride & Ambroxol Hydrochloride Tablets |
Each uncoated Tablet contains:
Paracetamol
Phenylephrine Hydrochloride
Guaiphenesin
Cetirizine Hydrochloride
Ambroxol Hydrochloride
Excipients
Approved colour used. |
IP
IP
IP
IP
IP |
325mg
5mg
50mg
5mg
15mg
q.s. |
693 |
Paracetamol, Phenylephrine Hydrochloride & Cetirizine Dihydrochloride Suspension |
Each 5ml contains:
Paracetamol
Phenylephrine Hydrochloride
Cetirizine Dihydrochloride
In a flavoured Syrupy Base.
Approved colour used.
(Banned drug 12/08/2024) |
IP
IP
IP |
125mg
5mg
2mg
q.s. |
694 |
Paracetamol, Phenylephrine Hydrochloride & Cetirizine Hydrochloride Suspension |
Each 5ml contains:
Paracetamol
Phenylephrine Hydrochloride
Cetirizine Hydrochloride
In a flavoured SyrupyBase.
Approved colour used.
(Banned drug 12/08/2024) |
IP
IP
IP |
125mg
2.5mg
2.5mg
q.s. |
695 |
Paracetamol, Phenylephrine hydrochloride & Cetirizine hydrochloride Tablets |
Each uncoated tablets contains:
Paracetamol
Phenylephrine hydrochloride
Cetirizine hydrochloride
Excipients
Approved colour used
(Banned drug 12/08/2024) |
IP
IP
IP |
500 mg
5 mg
5 mg
q.s. |
696 |
Paracetamol, Phenylephrine Hydrochloride & Chlorpheniramine MaleateSuspension |
Each 5ml Contains:
Paracetamol
Phenylephrine Hydrochloride
Chlorpheniramine Maleate
In a Flavoured Syrupy Base
Colour: Sunset Yellow FCF |
IP
IP
IP |
125mg
2.5mg
1mg
q.s |
697 |
Paracetamol, Phenylephrine Hydrochloride & Levocetirizine Dihydrochloride Tablets |
Each Uncoated Tablet Contains:
Paracetamol
Phenylephrine Hydrochloride
LevocetirizineDihydrochloride
Excipients
(Banned drug 12/08/2024) |
IP
IP
IP |
325mg
5mg
5mg
q.s. |
698 |
Paracetamol, Phenylephrine Hydrochloride, Cetirizine Hydrochloride , Dextromethorphan Hydrobromide & Caffeine Tablets |
Each uncoatedtablet contains :
Paracetamol
Phenylephrine Hydrochloride
Cetirizine Hydrochloride
Dextromethorphan Hydrobromide
Caffeine (Anhydrous)
Excipients
Approved colour used. |
IP
IP
IP
IP
IP |
500mg
10mg
5mg
10mg
30mg
q.s. |
699 |
Paracetamol, Phenylephrine Hydrochloride, Chlorpheniramine Maleate &Caffeine Tablets |
Each uncoated Tablet contains:
Paracetamol
Phenylephrine Hydrochloride
Chlorpheniramine Maleate
Caffeine (Anhydrous)
Excipients
Approved Colour Used. |
IP
IP
IP
IP |
325mg
5mg
2mg
15mg
q.s. |
700 |
Paracetamol, Phenylephrine Hydrochloride, Diphenhydramine Hydrochloride & Caffeine (Anhydrous) Tablets |
Each uncoated tablet contains:-
Paracetamol
Phenylephrine Hydrochloride
Diphenhydramine Hydrochloride
Caffeine (Anhydrous)
Excipients
Colour:-Approved colour used |
IP
IP
IP
IP |
500 mg
5 mg
25 mg
30 mg
q.s. |
701 |
Paracetamol, Phenylpherine Hydrochloride , Caffeine & Diphenhydra mine Hydrochloride Tablets |
Each uncoated tablet contains:
Paracetamol
Phenylpherine Hydrochloride
Caffeine (Anhydrous)
Diphenhydramine Hydrochloride
Excipients
Approved colour used. |
IP
IP
IP
IP |
325mg
5mg
30mg
25mg
q.s. |
702 |
Paracetamol& Dicyclomine Hydrochloride Suspension |
Each 5ml contains:
Paracetamol
Dicyclomine Hydrochloride
Flavoured Palatable Base
Colour: Sunset YellowFCF |
IP
IP |
125mg
5mg
q.s |
703 |
Paroxetine Hydrochloride Tablet |
Each film coated Tablet Contains :
Paroxetinehydrochloride Hemihydrate
Equ. to Paroxetine
Excipients
Approved Colour used |
IP |
20mg
q.s |
704 |
Paroxetine Prolonged Release tablet |
Each enteric–coated Bilayered prolonged release Tablet
contains :
Paroxetine Hydrochloride (as Hemihydrate)
Equ. to Paroxetine
Excipients
Approved colour used |
IP |
12.5mg
q.s |
705 |
Paroxetine Prolonged- Release Tablets IP |
Each enteric coated prolonged-release tablet
contains:
Paroxetine Hydrochloride Hemihydrate
Eq.to Paroxetine
Excipients
Approved colour used |
IP |
12.5mg |
706 |
Permethrin Lotion |
Composition :
Permethrin
Base |
|
5.0%w/v
q.s |
707 |
Phenylephrine Hydrochloride & Chlorpheniramine Maleate Syrup |
Each 5ml contains :
Phenylephrine hydrochloride
Chlorpheniramine Maleate
Flavoured syrupybase.
Approved colour used |
IP
IP |
5mg
2mg
q.s |
708 |
Phenylephrine Hydrochloride and Chlorpheniramine Maleate Drops IP |
Each ml contains :
Phenylephrine Hydrochloride
Chlorpheniramine Maleate
In a flavoured syrupy Base.
Approved colour used. |
IP
IP |
2.5mg
1mg
q.s. |
709 |
Phenylephrine Hydrochloride and Chlorpheniramine Maleate Drops IP |
Each ml contains :
Phenylephrine Hydrochloride
Chlorpheniramine Maleate
In a flavoured syrupyBase.
Approved colour used. |
IP
IP |
5mg
2mg
q.s. |
710 |
Phenylephrine Hydrochloride, Dextromethorphan Hydrobromide, Cetirizine Hydrochloride, Ambroxol Hydrochloride, Guaiphenesin Tablets |
Each uncoated Tablet Contains :
Phenylephrine Hydrochloride
Dextromethorphan Hydrochloride
Cetirizine Hydrochloride
Ambroxol Hydrochloride
Guaiphenesin
Excipients
Approved colour used. |
IP
IP
IP
IP
IP |
15mg
10mg
5mg
30mg
100mg
q.s. |
711 |
Phenylephrine Hydrochloride, Paracetamol & Cetirizine Hydrochloride Syrup |
Each 5ml Contains :
Phenylephrine Hydrochloride
Paracetamol
Cetirizine Hydrochloride
Flavoured Syrupy Base
Colour : Sunset Yellow FCF
(Banned drug 12/08/2024) |
IP
IP
IP |
5mg
125mg
5mg
q.s. |
712 |
Phenytoin Tablets IP |
Each film coated tablet contains:-
Phenytoin Sodium
Excipients
Colour : Approved Coloured Used |
IP |
100 mg
q.s. |
713 |
Piracetam & CiticolineTablet s |
Each film coatedtablet contain:
Piracetam
Citicoline Sodium
Eq. to Citicoline
Excipients
Approved colour used |
IP
IP |
400 mg
500 mg
q.s. |
714 |
Piracetam Tablets |
Each film coated tablet contains:
Piracetam
Excipients
Approved colour used |
IP |
800 mg
q.s. |
715 |
Piracetam Tablets IP |
Each film coatedtablet contain:
Piracetam
Excipients
Approved colour used |
IP |
400 mg
q.s. |
716 |
Piroxicame DispersibleTablets |
Each uncoated dispersible tablet contains:
Piroxicame
Excipients
Approved colour used |
IP |
20 mg
q.s. |
717 |
Posaconazole oral Suspension |
Each ml contains:
Posaconazole
Excipients
Approved Colour Used |
IP |
40mg
q.s |
718 |
Potassium Citrate and Citric Acid Oral Solution USP |
Each 5ml contains :
Potassium Citrate
Citric Acid Monohydrate
Flavoured Sorbitol Base.
Approved Colour Used |
IP
IP |
1100mg
334mg
q.s |
719 |
Potassium Citrate, Magnesium Citrate & Vitamin B6 Oral Solution |
Each 5ml contains :
Potassium Citrate
Magnesium Citrate
Pyridoxine Hydrochloride
In a Flavoured SyrupyBase
Approved colour used |
IP
USP
IP |
1100mg
375mg
20mg
q.s. |
720 |
Potassium Citrate, Magnesium Citrate & Vitamin B6 Oral Suspension |
Each 5ml contains :
Potassium Citrate
Magnesium Citrate
Pyridoxine Hydrochloride
In a Flavoured SyrupyBase
Approved colour used |
IP
USP
IP |
1100mg
375mg
20mg
q.s. |
721 |
Potassium Nitrate & Sodium Monofluorophosph ate Toothpaste |
Composition :
Potassium Nitrate
Sodium Monofluorophosphate
In a Pleasantly Flavoured Base
Colour :Brilliant Blue FCF |
BP
USP |
5.0%w/w
0.7%w/w
q.s |
722 |
Povidone –Iodine & Ornidazole Ointment |
Composition :
Povidone Iodine
(0.5% w/w Available Iodine)
Ornidazole
In an Ointment base |
IP
IP |
5.0%w/w
1.0%w/w
q.s |
723 |
Povidone Iodine GermicideGargle |
Composition:
Povidone Iodine
(0.2%w/vAvailable Iodine)
Absolute alcohol contain
In amint Flavour aqueous base |
IP |
2.0% w/v
8.38% v/v
q.s. |
724 |
Povidone Iodine ointment |
Composition :-
Povidone Iodine
Excipients |
IP |
5%w/w
q.s. |
725 |
Povidone Iodine Solution IP |
Composition :
Povidone Iodine
(available Iodine0.5%w/v)
Purified Water |
IP
IP |
5%w/v
q.s |
726 |
Povidone iodine, Metronidazole and Aloevera Ointment |
Composition
Povidoneiodine
(AvailableIodine0.5% w/w)
Metronidazole
Aloevera
Water Soluble ointment base.
(Banned drug 12/08/2024) |
IP
IP
IP |
5 % w/w
1 % w/w
1.50%w/w
q.s. |
727 |
Povidone Iodine& Metronidazole, Sucralfate Ointment. |
Composition :
Povidone Iodine
(available Iodine 0.5%w/w)
Metronidazole
Sucralfate
In a water soluble Ointment base. |
IP
IP
USP |
5.0 %W/W
1.0% W/W
7.0% W/W
q.s. |
728 |
Prasugrel Hydrochloride Tablets |
Each Film coated Tablet Contains :
Prasugrel Hydrochloride
Equ. to Prasugrel
Excipients
Approved colour used. |
|
5mg
q.s. |
729 |
Prasugrel Hydrochloride Tablets |
Each Film coated Tablet Contains :
Prasugrel Hydrochloride
Equ. to Prasugrel
Excipients
Approved colour used |
|
10mg
q.s. |
730 |
Prazosin Tablets IP |
Each uncoated tablet contains:
Prazosin Hydrochloride
Eq.to Prazosin
Excipients
Approved colour used. |
IP |
5mg
q.s. |
731 |
Pre & Probiotic With L-Glutamine Capsules |
Each hard gelatin capsule contains:
Fructo oligosaccharide
L- Glutamine
Bifidobecterium Bifidum
Bifidobecterium Longm
Lactobaccilus acidophillus
Streptococusthermophillus
Excipients
Approved colour used emptycapsule shells |
USP |
200 MG
100 mg
150million
150 million
300 million
150 million
q.s. |
732 |
Pre & Probiotic With ZincSachet |
Each 1 gm sachet contain:
Lactobacillus acidophilus
Lactobacillus rhamnosus
Lactobacillus casei
Lactobacillus plantarum
Lactobacillus bulgaricus
Bifidobacterium Longum
Bifidobacterium infantis
Bifidobacterium breve
Streptococcus Thermophillus
Fructo oligosaccharide
Zinc Sulphate Monohydrate
Eq. to elemental zinc
Saccharomyces boulardil
Excipients
Containspermitted synthetic flavours |
USP |
350 million
200 million
150 million
150 million 150
million
150 million
150 million
150 million
200 million
100 mg
10mg
0.05 billion
q.s. |
733 |
Prebiotic & Probiotic Capsules |
Each Hard Gelatin Capsule Contains:-
Fructooligosaccharides
Saccharomyces Boulardii
Bifidobacterium Bifidum
Bifidobacterium Longum
Lactobacillus Acidophillus
Streptococcus Thermophillus
Excipients
Approved colour used in empty capsule shells. |
|
200mg
250 million spores
150 million spores
150 million spores
300 million spores
150 million spores
q.s. |
734 |
Prednisolone Tablet IP |
Each uncoated Tablet contains:
Prednisolone
Excipients
Colour : Approved Coloured Used |
IP |
5mg
q.s |
735 |
Prednisolone Tablet IP |
Each uncoated Tablet contains:
Prednisolone
Excipients
Colour : Approved Coloured Used |
IP |
10mg
q.s |
736 |
Prednisolone Tablet IP |
Each uncoated Tablet contains
Prednisolone
Excipients
Colour : Approved Coloured Used |
IP |
20mg
q.s |
737 |
Pregabalin , Methylcobalamin, Alpha Lipoic Acid Pyridoxine with Folic Acid Capsules |
Each hard gelatin capsule contains
Pregabalin
Methylcobalamin
Alpha LipoicAcid
Pyridoxine Hydrochloride
Folic Acid
Excipients
Approved colour used in emptycapsule shells. |
IP
IP
USP
IP
IP |
75mg
750mcg
100mg
3mg
1.5mg
q.s |
738 |
Pregabalin (SR), Methylcobalamin & Nortriptyline Tablets |
Each film coated Tablet Contains:
Nortriptyline Hydrochloride
Equivalent to Nortriptyline
Pregabalin
(as Sustained Release)
Methylcobalamin
Excipient
Approved colour used |
IP
IP
IP |
10 mg
75 mg
1500mcg
q.s. |
739 |
Pregabalin (Sustained Release) & Methylcobalamin Tablets |
Each film coated Bilayered Tablet Contains:
Pregabalin
( As Sustained Release)
Methylcobalamin
Excipients
Approved Colour Used. |
IP
IP |
75mg
1500mcg
q.s. |
740 |
Pregabalin & Methylcobalamin Capsules IP |
Each hard gelatin capsule contains:- Pregabalin Methylcobalamin Excipients Approved colour used in emptycapsule shells. |
IP IP |
75 mg. 750 mcg. q.s. |
741 |
Pregabalin Capsules IP |
Each Hard Gelatin Capsule contains:
Pregabalin
Excipients
Approved colour used in EmptyHard Gelatin Capsule |
IP |
300mg
q.s |
742 |
Pregabalin Capsules IP |
Each Hard Gelatin Capsule contains:
Pregabalin
Excipients
Approved colour used in EmptyHard Gelatin Capsule |
IP |
75mg
q.s |
743 |
Pregabalin Capsules IP |
Each Hard Gelatin Capsule contains:
Pregabalin
Excipients
Approved colour used in EmptyHard Gelatin Capsule |
IP |
150mg
q.s |
744 |
Pregabalin Sustained Release Tablet |
Each Uncoated Sustained Release Tablet Contains :
Pregabalin
Excipients
Approved colour used |
IP |
75mg
q.s. |
745 |
Pregabalin, Methylcobalamin, Alpha Lipoic Acid, Folic acid & Pyridoxine Tablets |
Each film coated Tablet contains :
Pregabalin
Methylcobalamin
Alpha Lipoic Acid
Folic Acid
Pyridoxine hydrochloride
Excipients
Approved colour used |
IP
IP
USP
IP
IP |
75mg
1500mcg
100mg
1.5mg
3mg
q.s |
746 |
Pregabalin, Methylcobalamin, Benfotiamine, Pyridoxine Hydrochloride & Folic Acid Capsules |
Each Hard Gelatin Capsule Contains :
Pregabalin
Methylcobalamin
Benfotiamine
Pyridoxine Hydrochloride
Folic Acid
Excipients
Approved colour used in EmptyCapsule Shells |
IP
IP
IP
IP |
75mg
750mcg
7.5mg
1.5mg
0.75mg
q.s. |
747 |
Pregabalin( Sustained Release) & Methylcobalamin Tablets |
Each film coatedTablet Contains:
Pregabalin
( AsSustained Release)
Methylcobalamin
Excipients
Approved Colour Used. |
IP
IP |
75mg
1500mcg
q.s. |
748 |
Probiotic Capsules |
Each hard gelatin capsule contains:
Streptococcus Faecalis
Clostridium Butyricum
Bacillus Mesentericus
Lactic acid bacillus
(Lactobacillus sporogenes)
Excipients
Approved colour used. |
|
30 Million
2 Million
1 Million
50 Million
q.s. |
749 |
Prochlorperazine Maleate Mouth Dissolving Tablets |
Each uncoated Tablet contains:
Prochlorperazine Maleate
Excipients |
IP |
5mg
q.s. |
750 |
PromethazineSyrup |
Each 5ml Contains :
Promethazine Hydrochloride
Excipients
Colour : Approved Colour Used |
IP |
5mg |
751 |
Propranolol Hydrochloride (SR) & Flunarizine Tablets |
Each Uncoated Bilayered Tablet Contains:
Propranolol Hydrochloride
(as Sustained Release)
Flunarizine Dihydrochloride
Equ. To Flunarizine
Excipients
Approved colour used. |
IP
BP |
40mg
10mg
q.s. |
752 |
Propranolol Hydrochloride Tablets |
Each Uncoated Tablet Contains:
Propranolol Hydrochloride
Excipients |
IP |
40mg
q.s. |
753 |
Protein Hydrolysate, Calcium, Phosphorus, Vitamin B6, Cyanocobalamin Vitamin D3, Niacinamide, Folic Acid, Zinc & Iron |
Each 30g contains:
Protein hydrolysate 20%
Calcium
(as Dibasic Calcium Phosphate)
Phosphorus
(as Dibasic Calcium Phosphate)
Vitamin B6 (Pyridoxine Hydrochloride)
Vitamin B12 (Cyanocobalamin)
Vitamin D3
Niacinamide
Folic Acid
Zinc
(as ZincSulphate Heptahydrate IP)
Iron
(as Ferric Ammonium Citrate IP)
Excipients |
IP
IP
IP
IP
IP
IP
IP |
5 g
225 mg
174 mg
0.5 mg
1 mcg
100 IU
15 mg
300 mg
5 mg
7.5 mg
q.s. |
754 |
Prulifloxacin Tablets |
Each film coated Tablet Contains:
Prulifloxacin
Excipients
Approved Colour used |
|
600mg |
755 |
Pyridoxine Hydrochloride Tablets IP |
Each uncoated Tablet Contains:
Pyridoxine Hydrochloride
Excipients |
IP |
50mg
q.s. |
756 |
Rabeprazole & Domperidone Tablets |
Each entericcoatedtablets contains:
Rabeprazole Sodium
Domperidone
Excipients
Colour:-Approved colour used |
IP
IP |
20 mg
10 mg
q.s |
757 |
Rabeprazole Gastro- Resistant Tablets IP |
Each entericcoatedtablets contains:
Rabeprazole Sodium
Excipients
Colour:-Approved colour used |
IP |
20mg
q.s |
758 |
Rabeprazole sodium (Enteric coated) & Aceclofenac (Sustained Release) Capsule |
Each hardgelatin capsule contains:-
Rabeprazole Sodium
(Asa enteric coated Pellets)
Aceclofenac
(as a Sustainedrelease pellets)
Excipients
Approved colour used in emptycapsule shells |
IP
IP |
20mg
200mg
q.s |
759 |
Rabeprazole Sodium (Enteric coated) & Domperidone (Sustained Release) Capsules |
Each hard gelatin capsule contains:-
Rabeprazole Sodium
(As Enteric Coated Pellets)
Domperidone
(As Sustained Release Pellets)
Excipients
Approved colour used in emptycapsule shells. |
IP
IP |
20 mg
30 mg
q.s |
760 |
Rabeprazole Sodium (Enteric Coated) & Domperidone (Sustained Release) Capsules |
Each Hard Gelatin CapsuleContains
Rabeprazole Sodium
(As a EntericCoated Pellets)
Domperidone
(10mg Immediate Release Pellets)
(20mg Sustained Release Pellets)
Excipients
Approved colour used in emptycapsule shells |
IP
IP |
20mg
30mg
q.s. |
761 |
Rabeprazole sodium (Enteric coated) & Levosulpiride (Sustained release) capsule |
Each hard gelatin capsule contains:-
Rabeprazole Sodium
(AsEntericCoated Pellets)
Levosulpiride
(AsSustained ReleasePellets)
Excipients
Approved colour used in emptycapsule shells. |
IP
IP |
20 mg
75 mg
q.s |
762 |
Rabeprazole sodium (Enteric coated) And Itopride Hydrochloride (sustained Release) Capsules |
Each hard gelatin capsule contains:-
Rabeprazole Sodium
(Asa enteric coated Pellets)
Itopride Hydrochloride
(as a Sustainedrelease pellets)
Excipients
Approved colour used in emptycapsule shells. |
IP
IP |
20 mg
150 mg
q.s |
763 |
Rabeprazole Sodium 40mg (EC)& Domperidone 10(IR)20mg(SR) Capsules |
Each hard Gelatin Capsules Contains:
Rabeprazole Sodium
(as enteric coated pellets)
Domperidone
(as immediaterelease pellets)
Domperidone
(as sustained Release pellets)
Excipients
Approved Colour Used in emptyCapsules Shells |
IP
IP
IP |
40mg
10mg
20mg |
764 |
Racecadotril Capsules IP |
Each Hard Gelatin Capsules Contains:
Racecadotril
Excipients
Approved Colour used |
IP |
100mg |
765 |
Ramipril & Hydrochlorothiazid e Tablets IP |
Each uncoated Tablet Contains:
Ramipril
Hydrochlorthiazide
Excipients
Approved colour used |
IP
IP |
2.5mg
12.5mg
q.s. |
766 |
Ramipril & Hydrochlorothiazid e Tablets IP |
Each uncoated Tablet Contains:
Ramipril
Hydrochlorthiazide
Excipients
Approved colour used |
IP
IP |
5mg
12.5mg
q.s. |
767 |
Ramipril Tablets IP |
Each uncoated Tablet Contains:
Ramipril
Excipients
Approved colour used |
IP |
1.25 mg
q.s. |
768 |
Ramipril Tablets IP |
Each uncoated Tablet Contains:
Ramipril
Excipients
Approved colour used |
IP |
5mg
q.s. |
769 |
Ramipril Tablets IP |
Each Uncoated Tablet Contains:
Ramipril
Excipients |
IP |
2.5mg
q.s. |
770 |
Ranitidine Hydrochloride Tablets |
Each film coated Tablet contains:
Ranitidine Hydrochloride
Equ. to Ranitidine
Excipients
Approved colour used |
IP |
150mg
q. |
771 |
Ranitidine Hydrochloride Tablets |
Each film coated Tablet contains:
Ranitidine Hydrochloride
Equ. to Ranitidine
Excipients
Approved colour used. |
IP |
300mg
q.s |
772 |
Ranitidine Oral Solution IP |
Each 5ml Contains :
Ranitidine Hydrochloride
Equ. to Ranitidine
In a Flavoured SyrupyBase
Approved colour used |
IP |
75mg
q.s. |
773 |
Riboflavin , Folic Acid, Niacinamide & Lactic Acid Bacillus Tablets |
Each Uncoated Tablet contains:
Riboflavin
Folic acid
Niacinamide
Lacticacid bacillus
Excipients
Colour: Tartrazine |
IP
IP
IP |
10mg
1.5mg
100mg
60Million
Spores
q.s |
774 |
Riboflavin, Folic Acid, Niacinamide with Lactic Acid Bacillus Tablets |
Each uncoated Tablet Contains:
Riboflavin
Folic Acid
Niacinamide
Lactic Acid Bacillus
Excipients
Approved colour used. |
IP
IP
IP |
10mg
1.5mg
50mg
120 Million
spores
q.s. |
775 |
Rifaximin & Metronidazole Suspension |
Each 5 ml contains:
Rifaximin
Metronidazole Benzoate
Eq. to Metronidazole
In a flavoured base
Excipients
Approved colour used. |
I.P.
I.P. |
100mg
200mg
q.s. |
776 |
Rifaximin Oral Suspension |
Each 5ml contains:
Rifaximin
Excipients
Approved Colour Used. |
|
100mg
q.s. |
777 |
Rifaximin Tablets |
Each filmcoatedtablets contains:
Rifaximin
Excipients
Approved colour used |
|
550 mg
q.s. |
778 |
Rifaximin Tablets |
Each filmcoated tablets contains:
Rifaximin
Excipients
Approved colour used |
|
400 mg
q.s. |
779 |
RifaximineTablets |
Each filmcoated tablets contains:
Rifaximine
Excipients
Approved colour used |
|
200 mg
q.s. |
780 |
Rosuvastatin , Clopidogrel and Aspirin Capsule |
Each hard gelatin Capsule contains :
Rosuvastatin Calcium
Equ. to Rosuvastatin (as pellets)
Clopidogrel Bisulphate
Equ. to Clopidogrel (as pellets)
Aspirin
(as enteric coatedpellets)
Excipients
Approved colour used in emptycapsule shells. |
IP
IP
IP |
20mg
75mg
75mg
q.s. |
781 |
Rosuvastatin , Clopidogrel and Aspirin Capsules |
Each Hard Gelatin Capsule Contains :
Rosuvastatin Calcium
Equ. to Rosuvastatin(as pellets)
Clopidogrel Bisulphate
Equ. to Clopidogrel ( as pellets)
Aspirin
(as Enteric Coated Pellets)
Excipients
Approved colour used in emptyCapsule Shells |
IP
IP
IP |
10MG
75MG
75MG
q.s |
782 |
Rosuvastatin & Clopidogrel capsule |
Each hard gelatin capsule contains:
Rosuvastatin calcium
Equ. To Rosuvastatin
(as pellets Form)
Clopidogrel Bisulphate
Equ. To Clopidogrel
(as pellets Form)
Excipients
Approved colour used in emptycapsule shells. |
IP
IP |
10mg
75mg
q.s. |
783 |
Rosuvastatin & FenofibrateTablets |
Each film coated Tablet Contains:
Rosuvastatin Calcium
Equ. to Rosuvastatin
Fenofibrate
Excipients
Approved colour used |
IP
IP |
20mg
160mg
q.s. |
784 |
Rosuvastatin & FinofibrateTablet IP |
Each film coated tablet contains:-
Rosuvastatin calcium
Equ. toRosuvastatin
Finofibrate
Excipients
Colour : Approved Coloured Used |
IP
IP |
10mg
160mg
q.s. |
785 |
Rosuvastatin and Aspirin (EC) Capsules |
Each hard gelatin capsule contains:
Rosuvastatin Calcium
Equ. to Rosuvastatin
(In IR Pellets form)
Aspirin
(As enteric coated pellets)
Excipients
Approved Colour used in emptycapsules shells. |
IP
IP |
10mg
75mg |
786 |
Rosuvastatin and Aspirin (EC) Capsules |
Each hard gelatin capsule contains:
Rosuvastatin Calcium
Equ. to Rosuvastatin
(In IR Pellets form)
Aspirin
(As enteric coated pellets)
Excipients
Approved Colour used in emptycapsules shells. |
IP
IP |
20mg
75mg |
787 |
Rosuvastatin and Aspirin Capsules |
Each Hard Gelatin Capsule contain:
Rosuvastatin calcium
Equivalent to Rosuvastatin
(As pellets)
Aspirin
(As enteric coated pellets)
Excipients
Approved colour used in emptycapsule shells |
IP
IP |
10 mg
75 mg |
788 |
Rosuvastatin Tablet IP |
Each film coated tablet Contains :
Rosuvastatin Calcium
Equ. to Rosuvastatin
Excipients
Approved Colour Used |
IP |
40mg |
789 |
Rosuvastatin Tablets IP |
Each filmcoated tablet contain
Rosuvastatin Calcium
Eq.to Rosuvastatin
Excipients
Approved colour used |
IP |
5 mg
q.s. |
790 |
Rosuvastatin Tablets IP |
Each filmcoated tablet contain
Rosuvastatin calcium
Eq.to Rosuvastatin
Excipients
Approved colour used |
IP |
10 mg
q.s. |
791 |
Rosuvastatin Tablets IP |
Each filmcoated tablet contain
Rosuvastatin Calcium
Eq.to Rosuvastatin
Excipients
Approved colour used |
IP |
20 mg
q.s. |
792 |
Roxithromycin & Ambroxol Tablets |
Each film coatedtablet contain:
Roxithromycin
Ambroxol Hydrochloride
Excipients
Approved colour used |
IP
IP |
150 mg
60 mg
q.s |
793 |
Roxithromycin Tablets |
Each filmcoated tablets contains:
Roxithromycin
Excipients
Approved colour used |
IP |
150 mg
q.s. |
794 |
Serratiopeptidase tablet IP |
Each film coated tablet Contains:-
Serratiopeptidase
(Equ. toEnzyme activity20,000Units of enteric coated
granules)
Excipients
Colour : ApprovedColour Used |
IP |
10mg
q.s |
795 |
Sertraline Hydrochloride Tablets IP |
Each film coated Tablet Contains:
Sertraline Hydrochloride
Equ. To
Sertraline
Excipients
ApprovedColour used. |
IP |
50mg
q.s. |
796 |
Sertraline Tablets IP |
Each film coated tablets contains:
Sertraline Hydrochloride
Eq. to Sertraline
Excipients
Approved colour used. |
IP |
25mg
q.s. |
797 |
Sevelamer Carbonate Tablets |
Each film coated Tablet Contains:
Sevelamer Carbonate
Excipients
Approved colour used |
|
400mg
q.s. |
798 |
Sildenafil Citrate Tablets IP |
Each film coated tablet contains:-
Sildenafil Citrate
Eq. tosildenafil
Excipients
Colour:- Approved Colour used |
IP |
50 mg
q.s |
799 |
Sildenafil Citrate Tablets IP |
Each film coated tablet contains:-
Sildenafil Citrate
Eq. tosildenafil
Excipients
Colour:- Approved Colour used |
IP |
100 mg
q.s. |
800 |
Silodosin Capsules |
Each hard gelatin capsules contain:
Silodosin
Excipients |
|
8 mg
q.s. |
801 |
Silodosin Capsules |
Each hard gelatin capsules contain:
Silodosin
Excipients |
|
4 mg
q.s. |
802 |
Silver Nitrate, Chlorhexidine Gluconate, Aloevera & Allantoin Cream |
Composition :
Silver Nitrate
Chlorhexidine Gluconate Solution
Allantoin
AloeVera extract
Preservatives:
Chlorocresol
Cream Base |
IP
IP
IP
IP |
0.2%w/w
0.2%w/w
0.1%w/w
15.0%w/w
0.1%w/w
q.s |
803 |
Silver Sulphadiazine & Chlorhexidine GluconateCream |
Composition :
Silver Sulphadiazine
Chlorhexidine Gluconate solution
Equ. to Chlorhexidine
Cream base |
IP
IP |
0.5%w/w
0.2%w/w
q.s. |
804 |
Silymarin, L-Ornithine Laspartate, with B-Complex syrup |
Each 5ml contains :
Silymarin (80%)
L-Ornithine L- aspartate
Sorbitol solution (70%)
Vitamin B1
Vitamin B2
Vitamin B6
Vitamin B12
Niacinamide
Calcium D-Pantothenate
Flavoured Syrupy Base.
Approved Colour Used |
IP
IP
IP
IP
IP
IP
IP |
40mg
150mg
500mg
2.5mg
2.5mg
1.5mg
5mcg
25mg
5mg
q.s |
805 |
Simethicone , Dill Oil & Fennel Oil Drops |
Each ml contains:
Simethicone
Dill Oil
Fennel Oil
Flavoured palatable base.
Approved colour used |
IP
BP
IP |
40mg
0.005ml
0.0007ml
q.s. |
806 |
Simethicone, Norfloxacin & Metronidazole Suspension |
Each 5ml contains :
Simethicone
Norfloxacin
Metronidazole Benzoate
Equ. to Metronidazole
In a flavoured SyrupyBase
Approved colour used |
IP
IP
IP |
10mg
125mg
125mg
q.s. |
807 |
Sitagliptin Phosphate & Metformin Hydrochloride Tablets |
Each film coated Tablet Contains :
Sitagliptin Phosphate Monohydrate
Equ. to Sitagliptin
Metformin Hydrochloride
Excipients
Approved colour used. |
IP
IP |
64.25mg
50mg
850mg
q.s. |
808 |
Sitagliptin Phosphate & Metformin Hydrochloride Tablets |
Each film coated Tablets contains :
Sitagliptin Phosphate Monohydrate
Equ. to Sitagliptin
Metformin Hydrochloride
Excipients
Approved colour used |
IP |
64.25mg
50mg
500mg
q.s. |
809 |
Sitagliptin Phosphate & Metformin Hydrochloride Tablets |
Each film coated Tablets contains :
Sitagliptin Phosphate Monohydrate
Equ. to Sitagliptin
Metformin Hydrochloride
Excipients
Approved colour used |
IP |
64.25mg
50mg
1000mg
q.s. |
810 |
Sitagliptin PhosphateTablet |
Each film coated Tablet Contains :
Sitagliptin phosphate Monohydrate
Equ. to Sitagliptin
Excipients
Approved Colour used |
IP |
25mg
q.s |
811 |
Sitagliptin PhosphateTablet |
Each film coated Tablet Contains :
Sitagliptin phosphate Monohydrate
Equ. to Sitagliptin
Excipients
Approved Colour used |
IP |
50mg
q.s |
812 |
Sitagliptin PhosphateTablet |
Each film coated Tablet Contains :
Sitagliptin phosphate Monohydrate
Equ. to Sitagliptin
Excipients
Approved Colour used |
IP |
100mg
q.s |
813 |
Sodium Alginate, Sodium Bicarbonate & Calcium Carbonate Oral Suspension |
Each 5 ml contains:
Sodium Alginate
Sodium Bicarbonate
Calcium Carbonate
In a flavoured base.
Approved colour used |
IP
IP
IP |
250mg
133.5mg
80mg
q.s. |
814 |
Sodium Feredetate,Folic Acid,Cyanocoba lamin Syrup |
Each 5ml Contains:
SodiumFeredetate
(Eq. to33 mg.elemental Iron)
Folic Acid
Cyanocobalamin
Ina flavoured syrupy base
Approved colour use |
BP
IP
IP |
231mg
1.5mg
15mcg |
815 |
Sodium Picosulfate Oral Solution BP |
Each 5 ml contains:
Sodium Picosulfate
In a flavoured sorbitol base
Approved colour used |
BP |
5 mg
q.s. |
816 |
Sodium Valproate & Valproic Acid Controlled ReleaseTablet |
Each film coated controlledrelease tablet contains:
Sodium Valproate
Valproic Acid
(Both together correspond tosodium valproate)
Excipients
Approved colour used |
IP
IP |
133.5 mg
58 mg
200 mg
q.s. |
817 |
Sodium Valproate & Valproic Acid Controlled ReleaseTablet |
Each film coated controlledrelease tablet contains:
Sodium Valproate
Valproic Acid
(Both together correspond tosodium valproate)
Excipients
Approved colour used |
IP
IP |
333 mg
145 mg
500 mg
q.s. |
818 |
Solifenacin Succinate Tablets IP |
Each film coated tablet contains:
Solifenacin Succinate
Excipients
Approved colour used. |
IP |
5mg
q.s. |
819 |
Spironolactone Tablets IP |
Each Uncoated Tablet Contains:
Spironolactone
Excipients
Approved colour used |
IP |
25mg
q.s. |
820 |
Spironolactone Tablets IP |
Each Uncoated Tablet Contains:
Spironolactone
Excipients
Approved colour used |
IP |
50mg
q.s. |
821 |
Spironolactone Tablets IP |
Each Uncoated Tablet Contains:
Spironolactone
Excipients
Approved colour used |
IP |
100mg
q.s. |
822 |
Sucralfate & Oxetacaine Oral suspension |
Each 10ml Contains:-
Sucralfate
Oxetacaine
In palatable sorbitol Base
Approved Colour Used. |
USP
BP |
1g.
20mg.
q.s. |
823 |
Sucralfate & Oxetacaine Suspension |
Each 5ml contains:
Sucralfate
Oxetacaine
In a flavoured syrupyBase.
Approved colour used. |
USP
BP |
500mg
10mg
q.s. |
824 |
Sucralfate & Oxetacaine Suspension |
Each 10ml contains:
Sucralfate
Oxetacaine
In a flavoured palatable base
Approved colour used |
IP
BP |
1g
10 mg
q.s. |
825 |
Sucralfate & Oxetacaine Suspension |
Each 5ml contains:
Sucralfate
Oxetacaine
In a flavoured palatable base
Approved colour used |
USP
BP |
1g
10 mg
q.s. |
826 |
Sucralfateand Oxetacaine Suspension |
Each 10ml contain:
Sucralfate
Oxetacaine
In a flavoured sorbitol base
Approved colour used |
IP
BP |
IP
BP |
827 |
Sulfasalazine Gastro –Resistant Tablets IP |
Each enteric coated tablet contains:
Sulfasalazine
Excipients
Approved colour used. |
IP |
500mg
q.s. |
828 |
Sulfasalazine Gastro Resistant Tablets USP |
Each Enteric Coated Tablet Contains:
Sulfasalazine
Excipients
Approved colour used |
USP |
1000mg
q.s. |
829 |
Syrup of Iron, Folic Acid & Vitamin B12 with Minerals |
Each 15ml contains :
Ferric Ammonium Citrate
Cyanocobalamin
Folic Acid
Copper Sulphate
Manganese Sulphate
In a Flavoured Syrupybase.
Approved colour Used. |
IP
IP
IP
BP
BP |
160mg
7.5mcg
7.5mg
30mcg
30mcg
q.s. |
830 |
Syrup of vitamin iron ,folicacid, zinc with Cyanocobalamin. |
Each 15ml contains:
FerricAmmonium citrate
(equivalent to32.25mgElemental Iron)
Cyanocobalamin
Folic acid
ZincSulphate
(equivalent to7.5mg ofElement Zinc )
Flavored syrup base
Approved Colour Used |
IP
IP
IP
IP |
150mg
15mcg
1.5mg
33mg
q.s. |
831 |
Tablets of Biotin, N-Acetyl L- Cysteine, Vitamins & Minerals |
Each film coated tablet contains:
Biotin
N-Acetyl L- Cysteine
Calcium Pantothenate
Sodium selenite
eq.to elemental Selenium
Cupric Oxide
eq.to elemental Copper
Zinc Oxide
eq. to elemental Zinc
Manganese Sulphate
eq. to elemental Manganese
Folic Acid
Excipients
Approved colour used.
Appropriate overages of vitamins added to
compensate
Loss on storage
For Therapeutic use only |
IP
BP
IP
BP
IP
BP
IP |
10mg
50mg
100mg
65mcg
3mg
25mg
1mg
1mg
q.s. |
832 |
Tacrolimus cream |
Composition:-
Tacrolimus
Excipients |
IP |
0.1%w/w
q.s. |
833 |
Tadalafil Tablet IP |
Each uncoated tablet contains:
Tadalafil
Excipients
Approved colour used |
IP |
10 mg
q.s |
834 |
Tadalafil Tablet IP |
Each uncoated tablet contains:
Tadalafil
Excipients
Approved colour used |
IP |
20 mg
q.s |
835 |
Tamsulosin Hydrochloride (MR) & Dutasteride Tablets |
Each film coated Tablet contains:
Tamsulosin Hydrochloride
(as modified release)
Dutasteride
Excipients
Approved colour used. |
IP
IP |
0.4 mg
0.5 mg
q.s. |
836 |
Tamsulosin Hydrochloride Modified Release Tablets |
Each film coated Tablet contains:
Tamsulosin Hydrochloride
(as modified release)
Excipients
Approved colour used. |
IP |
0.4mg
q.s. |
837 |
Tapentadol Tablets |
Each film coatedtablet contain:
Tapentadol Hydrochloride
Equivalent to Tapentadol
Excipients
Approved colour used |
IP |
50 mg
q.s. |
838 |
Tapentadol Tablets |
Each film coatedtablet contain:
Tapentadol Hydrochloride
Equivalent to Tapentadol
Excipients
Approved colour used |
IP |
100 mg
q.s. |
839 |
Telmisartan & AmlodipineTablets |
Each uncoated Bilayered Tablet Contains:
Telmisartan
Amlodipine Besylate
Equ. To
Amlodipine
Excipients
Approved colour used |
IP
IP |
80mg
5mg
q.s. |
840 |
Telmisartan & AmlodipineTablets IP |
Each Uncoated Tablet Contains:-
Telmisartan
Amlodipine Besylate
Equ. To Amlodipine
Excipients
Colour: Approved Coloured Used |
IP
IP |
80mg
10mg
q.s |
841 |
Telmisartan & AmlodipineTablets IP |
Each Uncoated Tablet Contains :-
Telmisartan
Amlodipine Besylate
Equ. To Amlodipine
Excipients
Colour: Approved Colour Used. |
IP
IP |
40mg
5mg
q.s. |
842 |
Telmisartan & AmlodipineTablets IP |
Each Uncoated Tablet Contains :-
Telmisartan
Amlodipine Besylate
Equ. To Amlodipine
Excipients
Approved Colour Used. |
IP
IP |
80mg
5mg
q.s. |
843 |
Telmisartan & AmlodipineTablets IP |
Each Uncoated Bilayered Tablet Contains :-
Telmisartan
Amlodipine Besylate
Equ. To Amlodipine
Excipients
Colour: Approved Colour Used. |
IP
IP |
40mg
5mg
q.s. |
844 |
Telmisartan & AmlodipineTablets IP |
Each Uncoated Bilayered Tablet Contains:-
Telmisartan
Amlodipine Besylate
Equ. To Amlodipine
Excipients
Colour: Approved Coloured Used. |
IP
IP |
80mg
10mg
q.s |
845 |
Telmisartan & Atorvastatin Tablets |
Each film coated Tablet Contains :
Telmisartan
Atorvastatin Calcium
Equ. to Atorvastatin.
Excipients
Approved colour used. |
IP
IP |
40mg
10mg
q.s. |
846 |
Telmisartan & Chlorthalidone Tablets |
Each uncoated Bilayered Tablet contains:
Telmisartan
Chlorthalidone
Excipients
Approved colour used |
IP
IP |
40mg
12.5mg
q.s. |
847 |
Telmisartan & CilnidipineTablets |
Each Film coated Tablet Contains :
Telmisartan
Cilnidipine
Excipients
Approved colour used. |
IP
IP |
40mg
10mg
q.s. |
848 |
Telmisartan & Hydrochlorthiazide Tablet IP |
Each Uncoated Tablet Contains:-
Telmisartan
Hydrochlorothiazide
Excipients
Colour: Approved Coloured Used. |
IP
IP |
80mg
12.5mg
q.s |
849 |
Telmisartan & Metoprolol Succinate (ER) Tablets |
Each Uncoated Bilayered Tablet Contains:
Telmisartan
Metoprolol Succinate
Equ. to Metoprolol Tartrate
(as Extended Release )
Excipients
Approved colour used |
IP
IP
IP |
40mg
23.75
25mg
q.s. |
850 |
Telmisartan & Metoprolol Succinate (ER) Tablets |
Each uncoated bilayer tablet contain:
Telmisartan
Metoprolol Succinate
Eq. to Metoprolol Tartrate
(As Extended Release)
Excipients
Approved colour used |
IP
IP |
40 mg
47.5 mg
50 mg
q.s. |
851 |
Telmisartan and Hydrochlorothiazid e TabletsIP |
Each Uncoated Tablet Contains:-
Telmisartan
Hydrochlorothiazide
Excipients
Colour: ApprovedColour Used. |
IP
IP |
40mg
12.5mg
q.s. |
852 |
Telmisartan Tablet IP |
Each Uncoated Tablet Contains:-
Telmisartan
Excipients
Colour: Approved Colour Used. |
IP |
20mg
q.s |
853 |
Telmisartan Tablet IP |
Each Uncoated Tablet Contains:-
Telmisartan
Excipients
Colour: Approved Colour Used. |
IP |
40mg
q.s |
854 |
Telmisartan Tablet IP |
Each Uncoated Tablet Contains:-
Telmisartan
Excipients
Colour: Approved Colour Used. |
IP |
80mg
q.s |
855 |
Telmisartan, Amlodipine & Hydrochlorothiazid e |
Each uncoated bilayer tablet contain:
Telmisartan
Amlodipine Besylate
Eq.to Amlodipine
Hydrochlorothiazide
Excipients
Approved colour used |
IP
IP
IP |
40 mg
5 mg
12.5 mg |
856 |
Teneligliptin & Metformin Hydrochloride Tablets |
Each uncoated bilayered tablet contains:
Teneligliptin Hydrobromide hydrate
Equivalent to Teneligliptin
Metformin hydrochloride
(As Extended release)
Excipients
Approved colour used |
IP |
20 mg
1000 mg
q.s. |
857 |
Teneligliptin & Metformin hydrochloride Tablets |
Each uncoated by-layered tablets contains:
Teneligliptin hydrobromide hydrat
Equivalent to Teneligliptin
Metformin hydrochloride
(As Extended release)
Excipients
Approved colour used |
IP |
20 mg
500 mg
q.s. |
858 |
Terbinafine Hydrochloride Cream IP |
Composition:
Terbinafine Hydrochloride
Preservatives
Benzyl Alcohol
In a Cream Base |
IP
IP |
1%w/w
1%w/w
q.s. |
859 |
Terbinafine hydrochloride Tablets IP |
Each filmcoated tablets contains:
Terbinafine hydrochloride
Equivalent to Terbinafine
Excipients
Approved colour used |
IP |
250 mg
q.s. |
860 |
Terbinafine hydrochloride Tablets IP |
Each film coated tablets contains:
Terbinafine hydrochloride
Equivalent to Terbinafine
Excipients
Approved colour used |
IP |
500 mg
q.s. |
861 |
Terbutaline , Bromhexine, Guaiphenesin and Menthol Syrup |
Each 5ml contains :
Terbutaline Sulphate
Bromhexinehydrochloride
Guaiphenesin
Menthol
In a Flavoured SyrupyBase
Approved colour used |
IP
IP
IP
IP |
1.25mg
2mg
50mg
0.5mg |
862 |
Terbutaline Sulphate & Bromhexine Hydrochloride Syrup |
Each 5ml contains :
Terbutaline Sulphate
Bromhexine Hydrochloride
In a Flavoured palatable base.
Approved colour used |
IP
IP |
2.5mg
8mg
q.s. |
863 |
Terbutaline Sulphate & Choline Theophyllinate Syrup |
Each 5ml contains :
Terbutaline Sulphate
CholineTheophyllinate
In a flavoured SyrupyBase.
Approved colour Used. |
IP
BP |
1.25mg
50mg
q.s. |
864 |
Terbutaline Sulphate, Ambroxol HCl, Guaiphenesin & Menthol Expectorant |
Each 5ml contains :
Terbutaline Sulphate
Ambroxol Hydrochloride
Guaiphenesin
Menthol
Flavoured SyrupyBase
Approved colour used. |
IP
IP
IP
IP |
1.5mg
15mg
50mg
1.5mg
q.s. |
865 |
Terbutaline Sulphate, Ambroxol HCl, Guaiphenesin & Menthol Expectorant |
Each 5ml contains :
Terbutaline Sulphate
Ambroxol Hydrochloride
Guaiphenesin
Menthol
Flavoured SyrupyBase
Approved colour used. |
IP
IP
IP
IP |
1.5mg
15mg
50mg
1.5mg
q.s. |
866 |
Terbutaline Sulphate, Bromhexine HCL, Guaiphenesin & Menthol Syrup |
Each 5ml Contains
Terbutaline Sulphate
Equivalent to Terbutaline
Bromhexine Hydrochloride
Guaiphenesin
Menthol
In flavoured Syrupybase
Approved colour used |
IP
IP
IP
IP |
1.25 mg
2 mg
50mg
0.5 mg
q.s. |
867 |
Terbutaline Sulphate, Guaiphenesin, Ambroxol Hydrochloride & Menthol Syrup |
Each 5ml contains :
Terbutaline Sulphate
Guaiphenesin
Ambroxol Hydrochloride
Menthol
In a Flavoured syrupyBase
Approved colour used |
IP
IP
IP
IP |
1.25mg
50mg
15mg
0.5mg
q.s. |
868 |
Thiamine Hydrochloride Tablets IP |
Each film coated Tablet Contains:
Thiamine Hydrochloride
Excipients
Approved colour used |
IP |
100mg
q.s. |
869 |
Thiamine Tablets IP |
Each uncoated Tablet Contains
Thiamine Hydrochloride
Excipients
Colour :- Approved colour used |
IP |
50mg
q.s |
870 |
Thiocolchicoside Capsules |
Each Hard Gelatin Capsule Contains :
Thiocolchicoside
Excipients
Approved colour used in EmptyCapsule shells |
IP |
4mg
q.s. |
871 |
Thymol, Menthol, Eucalyptol & Ethanol Mouthwash |
Composition :
Thymol
Menthol
Eucalyptol
Ethanol(95%)
Approved Colour Used |
IP
IP
IP |
0.06%w/v
0.04%w/v
0.09%w/v
21.6%v/v |
872 |
Thyroxine Tablet IP |
Each Uncoated Tablet Contains
Thyroxine sodium
(as anhydrous)
Excipients
Colour : Approved Coloured Used |
IP |
12.5mcg
q.s |
873 |
Thyroxine Tablet IP |
Each Uncoated Tablet Contains
Thyroxine sodium
(as anhydrous)
Excipients
Colour : Approved Coloured Used |
IP |
25mcg
q.s |
874 |
Thyroxine Tablet IP |
Each Uncoated Tablet Contains
Thyroxine sodium
(as anhydrous)
Excipients
Colour : Approved Coloured Used |
IP |
50mcg
q.s |
875 |
Thyroxine Tablet IP |
Each Uncoated Tablet Contains
Thyroxine sodium
(as anhydrous)
Excipients
Colour : Approved Coloured Used |
IP |
75mcg
q.s |
876 |
Thyroxine Tablet IP |
Each Uncoated Tablet Contains
Thyroxine sodium
(as anhydrous)
Excipients
Colour : Approved Coloured Used |
IP |
100 mcg
q.s |
877 |
Ticagrelor Tablets |
Each film coated tablet contains:
Ticagrelor
Excipients
Approved colour used |
IP |
90mg
q.s |
878 |
Tolperisone Hydrochloride & Diclofenac Sodium Tablets |
Each Film coated Tablets Contains :
Tolperisone Hydrochloride
Diclofenac Sodium
Excipients
Approved colour used |
IP
IP |
150mg
50mg
q.s. |
879 |
Tolperisone Hydrochloride & Paracetamol Tablet |
Each film coated Tablet Contains:
Tolperisone hydrochloride
Paracetamol
Excipients
Approved colour Used |
JP
IP |
150mg
325mg |
880 |
Tolperisone Hydrochloride Sustained Release Tablet |
Each film coated sustained Release Tablet Contains:
Tolperisone Hydrochloride
Excipients
Approved Colour Used |
JP |
450mg |
881 |
Tolperisone Hydrochloride Tablet |
Each film coated Tablet Contains:
Tolperisone Hydrochloride
Excipients
Approved colour used |
JP |
150mg
q.s |
882 |
Torsemide & Spironolactone Tablets |
Each uncoated tablet contains:
Torsemide
Spironolactone
Excipients
Approved colour used |
IP
IP |
5 mg
50 mg
q.s. |
883 |
Torsemide & Spironolactone Tablets |
Each uncoated tablet contain:
Torsemide
Spironolactone
Excipients
Approved colour used |
IP
IP |
10 mg
50 mg
q.s. |
884 |
Torsemide & Spironolactone Tablets |
Each uncoated tablet contain:
Torsemide
Spironolactone
Excipients
Approved colour used |
IP
IP |
20 mg
50 mg
q.s. |
885 |
Torsemide Tablets IP |
Each uncoated tablet contain:
Torsemide
Excipients
Approved colour used |
IP |
10 mg
q.s. |
886 |
Torsemide Tablets IP |
Each uncoated tablet contain:
Torsemide
Excipients
Approved colour used |
IP |
20 mg
q.s. |
887 |
Torsemide Tablets IP |
Each uncoated tablet contain:
Torsemide
Excipients
Approved colour used |
IP |
5 mg
q.s. |
888 |
Torsemide Tablets IP |
Each uncoated tablet contain:
Torsemide
Excipients
Approved colour used |
IP |
100 mg
q.s. |
889 |
Tramadol & ParacetamolTablet |
Each Film Coated Tablet Contains:
Paracetamol
Tramadol Hydrochloride
Excipients
Approved Colour Used |
IP
IP |
325mg
37.5mg
q.s |
890 |
Tramadol Hydrochloride Prolonged Release Tablet IP |
Each film coated sustainedrelease tablet contain:
Tramadol Hydrochloride
Excipients
Approved colour used |
IP |
100mg
q.s |
891 |
Tramadol Hydrochloride Tablet IP |
Each film coatedtablet contain:
Tramadol Hydrochloride
Excipients
Approved colour used |
IP |
100mg
q.s |
892 |
Tranexamic Acid & Ethamsylate Tablets |
Each film coated Tablet contains:
Tranexamic Acid
Ethamsylate
Excipients
Approved colour used. |
IP
BP |
250mg
250mg
q.s. |
893 |
Tranexamic Acid Tablets |
Each film coated Tablet Contains:
Tranexamic Acid
Excipients
Colour : Approved Coloured Used |
BP |
250mg
q.s |
894 |
Tranexamic Acid Tablets IP |
Each film coated Tablet Contains:
Tranexamic Acid
Excipients
Colour : Approved Coloured Used |
IP |
250mg
q.s |
895 |
Tranexamic Acid Tablets IP |
Each film coated Tablet Contains:
Tranexamic Acid
Excipients
Approved Colour Used. |
IP |
500mg |
896 |
TranexamicAcid& Mefenamic Acid Tablets |
Each filmcoated tablets contains:
Tranexamic Acid
Mefenamic Acid
Excipients
Approved colour used |
IP
IP |
500 mg
250 mg
q.s. |
897 |
Tricholine Citrate & Sorbitol Solution Syrup |
Each 10 ml contains:
Tricholine Citrate
Sorbitol Solution (70%)
(Non-Crystallising)
Excipients
Approved colour used. |
IP |
0.55gm
7.150gm
q.s. |
898 |
Trifluoperazine Hydrochloride Tablets IP |
Each film coated Tablet contains:
Trifluoperazine Hydrochloride
Excipients
Approved colour used |
IP |
5mg
q.s |
899 |
Troxerutin, Calcium Dobesilate, Zinc, Phenylephrine, Lignocaine with Hydrocortisone Cream |
Composition :
Troxerutin
Calcium Dobesilate Monohydrate
Equ. to Anhydrous Calcium Dobesilate
Lignocaine Hydrochloride
Hydrocortisone Acetate
Zinc Oxide
Phenylephrine Hydrochloride
Cream Base |
BP
BP
IP
IP
IP
IP |
2.0%w/w
0.25%w/w
3.0%w/w
0.25%w/w
5.0%w/w
0.1%w/w
q.s |
900 |
Trypsin – Chymotrypsin Tablets |
Each enteric - coated tablet contains:
2,00,000 Armour Units of Enzymatic Activity*
*Supplied by a purified Concentrate which has Specific
Trypsin and Chymotrypsin Activity in a Ratio of
Approximately Six to One.
Excipients
Approved colour used. |
|
2,00,000 AU
q.s. |
901 |
Trypsin , Bromelain and Rutoside Trihydrate Tablets |
Each Enteric coated tablet contains:
Trypsin
Bromelain
RutosideTrihydrate
Excipients
Approved colour used. |
BP
BP |
96mg
180mg
200mg
q.s. |
902 |
Trypsin- Chymotrypsin Tablets |
Each entericcoated Tablet contains:
1,00,000 Armour units of enzymaticactivity
*Supplied by a purified concentrate which has specific
Trypsin & Chymotrypsin activityin aratio of Approximately
six to one.
Excipients
Approved colour used. |
q.s. |
|
903 |
Trypsin-Chymotrypsin, Aceclofenac & Paracetamol Tablets |
Each film coated tablet contains:
Aceclofenac
Paracetamol
Trypsin-Chymotrypsin
Of enzyme activity (as enteric coated granules)
Excipients
Approved colour used. |
I.P.
I.P. |
100mg
325mg
150,000AU
q.s. |
904 |
Trypsin, Bromelain & Rutoside Trihydrate Tablets |
Each Enteric coatedTablet Contains:-
Trypsin
Bromelain
RutosideTrihydrate
Equivalent toRutoside (anhydrous)
Excipients
Approved colour used |
BP
BP |
48 mg
90 mg
100 mg
q.s. |
905 |
Trypsin, Bromelain, Rutoside Trihydrate & Diclofenac Sodium Tablets |
Each Enteric coatedTablet Contains:
Trypsin
Bromelain
Rutoside Trihydrate
Diclofenac Sodium
Excipients
Approved Colour Used |
BP
BP
IP |
48mg
90mg
100mg
50mg
q.s. |
906 |
Trypsin, Bromelain, Rutoside Trihydrate and Aceclofenac Tablets |
Each enteric coated Tablet contains :
Trypsin
Bromelain
Rutoside Trihydrate
Aceclofenac
Excipients
Approved colour used |
IP
BP
IP |
48mg
90mg
100mg
100mg
q.s |
907 |
Urea, Lactic acid, Propylene Glycol & Liquid Paraffin Cream |
Composition :
Urea
Lactic Acid
Propylene Glycol
Liquid Paraffin
Preservatives:
Methyl Paraben
Propyl Paraben
Cream Base |
IP
IP
IP
IP
IP
IP |
10%w/w
10%w/w
10%w/w
10%w/w
0.16%w/w
0.04%w/w
q.s |
908 |
Ursodeoxycholic Acid Tablets IP |
Each filmcoated tablets contains:
Ursodeoxycholic Acid
Excipients
Approved colour used |
IP |
300 mg
q.s. |
909 |
Ursodeoxycholic Acid Tablets IP |
Each film coated tablets contains:
Ursodeoxycholic Acid
Excipients
Approved colour used |
IP |
150 mg
q.s. |
910 |
Ursodeoxycholic Oral Acid Suspension |
Each 5ml Contains :
Ursodeoxycholic Acid
Excipients
Approved colour used |
IP |
125mg
q.s. |
911 |
Ursodeoxycholic Oral Acid Suspension |
Each 5ml Contains :
Ursodeoxycholic Acid
Excipients
Approved colour used |
IP |
250mg
q.s. |
912 |
Vildagliptin & Metformin Hydrochloride Tablet |
Each film coated tablet contains:
Vildagliptin
Metformin Hydrochloride
Excipients
Approved colour used |
IP |
50 mg
500 mg
q.s. |
913 |
Vildagliptin & Metformin Hydrochloride Tablet |
Each film coated tablet contains:
Vildagliptin
Metformin Hydrochloride
Excipients
Approved colour used |
IP |
50 mg
1000 mg
q.s. |
914 |
Vildagliptin Tablet |
Each uncoatedtablet contains:
Vildagliptin
Excipients
Approved colour used |
|
50 mg
q.s. |
915 |
Virgin Linseed Oil, Diclofenac Diethylamine, Methyl Salicyclate, Menthol& Capsaicin Gel |
Composition:
Virgin Linseed Oil
Diclofenac Diethylamine
Equ. to Diclofenac Sodium
Methyl Salicyclate
Menthol
Capsaicin
Preservative :
Benzyl Alcohol
Gel Base |
BP
IP
IP
IP
USP
IP |
3.00%w/w
1.16%w/w
1.00%w/w
10.00%w/w
5.00%w/w
0.025%w/w
1.00%w/w
q.s. |
916 |
Vitamin B6, Nicotinamide, Vitamin B12 & Lysine Syrup |
Each 5ml contains :
Pyridoxine Hydrochloride
Nicotinamide
Cyanocobalamin
L-Lysine Hydrochloride
Sorbitol Solution (70%)
(Non-Crystallizing)
Colour: Caramel |
IP
IP
IP
USP
IP |
0.75mg
15mg
2mcg
37.5mg
q.s |
917 |
Vitamin D3 oral Drops |
Each ml contains:
Cholecalciferol
(Vitamin D3 as stabilized)
In a flavoured syrupybase
Approved colour used. |
IP |
800IU
q.s. |
918 |
Vitamin D3 oral solution |
Each 5 ml contains:
Cholecalciferol
(In Nano Droplet form)
In a flavoured sugar free syrupybase.
Approved colour used. |
IP |
60000IU
q.s |
919 |
Vitamin E Acetate & Levocarnitine Tablets |
Each film coated tablet contains:
Tocopheryl Acetate
(as 50% powder)
L- Carnitine –L – Tartrate
Eq. to Levocarnitine
Appropriate overages added
Excipients
Approved colour used. |
IP
USP |
200mg
150mg
q.s |
920 |
Voglibose & Metformin Hydrochloride (Sustained Release) Tablet |
Each uncoated Bilayered tablet contains:
Voglibose
Metformin Hydrochloride
(As Sustained Release)
Excipients
Approved colour used |
IP
IP |
0.2 mg
500 mg
q.s. |
921 |
Voglibose & Metformin Hydrochloride (Sustained Release) Tablet |
Each uncoated Bilayered tablet contains:
Voglibose
Metformin Hydrochloride
(As Sustained Release)
Excipients
Approved colour used |
IP
IP |
0.3 mg
500 mg
q.s. |
922 |
Voglibose Dispersible Tablet IP |
Each uncoated tablet contains:
Voglibose
Excipients
Approved colour used |
IP |
0.2 mg
q.s. |
923 |
Voglibose Dispersible Tablet IP |
Each uncoated tablet contains:
Voglibose
Excipients
Approved colour used |
IP |
0.3 mg
q.s. |
924 |
Voglibose, Glimepiride & Metformin Hydrochloride (Sustained Release) Tablet |
Each uncoated Bilayered tablet contains:
Voglibose
Glimepiride
Metformin Hydrochloride
(As Sustained Release)
Excipients
Approved colour used |
IP
IP
IP |
0.3 mg
2 mg
500 mg
q.s. |
925 |
Voglibose, Glimepiride & Metformin Hydrochloride (Sustained Release) Tablet |
Each uncoated Bilayered tablet contains:
Voglibose
Glimepiride
Metformin Hydrochloride
(As Sustained Release)
Excipients
Approved colour used |
IP
IP
IP |
0.2 mg
1 mg
500mg
q.s. |
926 |
Voglibose, Glimepiride & Metformin Hydrochloride (Sustained Release) Tablet |
Each uncoated Bilayered tablet contains:
Voglibose
Glimepiride
Metformin Hydrochloride
(As Sustained Release)
Excipients
Approved colour used |
IP
IP
IP |
0.2 mg
2 mg
500mg
q.s. |
927 |
Voriconazole Tablet IP |
Each film coated Tablet Contains:
Voriconazole
Excipients
Approved Colour Used. |
IP |
200 mg
q.s |
928 |
Warfarin Sodium Tablets IP 1mg |
Each uncoated tablet contains:
Warfarin Sodium Clathrate
Eq. to Warfarin Sodium
(anhydrous)
Excipients
ApprovedColour used |
IP |
1mg
q.s. |
929 |
Warfarin Sodium Tablets IP 3mg |
Each uncoated tablet contains:
Warfarin Sodium Clathrate
Eq. to Warfarin Sodium
(anhydrous)
Excipients
Approved Colour used |
IP |
3mg
q.s. |
930 |
Warfarin Sodium Tablets IP 5mg |
Each uncoated tablet contains:
Warfarin Sodium Clathrate
Eq. to Warfarin Sodium
(anhydrous)
Excipients
Approved Colour used |
IP |
5mg
q.s. |
931 |
WhiteSoft Paraffin & Light Liquid Paraffin Cream |
Composition :
White Soft Paraffin
Light Liquid Paraffin
Cream Base |
IP
IP |
13.2%w/w
10.2%w/w
q.s |
932 |
Zinc Acetate Oral Solution USP |
Each 5 ml contains:
Zinc Acetate (as Dihydrate)
Eq.to Elemental Zinc
In a Mentholated Syrupy base.
Approved colour used. |
USP |
20mg
q.s. |
933 |
Zinc Acetate Syrup |
Each 5ml contains :
Zinc Acetate (as Dihydrate)
Equ. to Elemental Zinc
In a Mentholated SyrupyBase.
Approved Colour used. |
USP |
20mg
q.s. |
934 |
Zinc Acetate Tablets |
Each Enteric coated Tablet Contains:
Zinc Acetate(as dihydrate)
Equ. toElemental Zinc
Excipients
Approved Colour Used |
USP |
50mg
q.s |
935 |
Zinc gluconate Oral Solution |
Each 5ml contains:
Zinc gluconate
Eq. to elemental zinc
In a flavoured syrupy base
Approved colour used. |
USP |
20mg
q.s |
936 |
ZincGluconate Suspension |
Each 5ml contains:
Zinc Gluconate
Equ. to Elemental Zinc
In a flavoured SyrupyBase
Colour: Ponceau 4R |
USP |
20mg
q.s |
937 |
ZincSulphateOral Solution IP |
Each 5 ml Contains:
Zinc Sulphate
Equivalent to elemental zinc
In a Flavoured palatable base
Approved colour used |
IP |
20 mg
q.s. |