1 |
Acebrophylline & Acetylcysteine Tablets |
Each film coated Tablet Contains:
Acebrophylline
Acetylcysteine
Excipients
Approved colour used. |
BP |
100mg
600mg
q.s. |
2 |
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. |
3 |
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. |
4 |
Acebrophylline Sustained Release Tablets |
Each film coated sustained release Tablet contains :
Acebrophylline
Excipients
Approved colour used |
|
200mg
q.s. |
5 |
Acebrophylline Sustained Release Tablets |
Each film coated sustained release Tablet contains :
Acebrophylline
Excipients
Approved colour used |
|
200mg
q.s. |
6 |
Aceclofenac & DrotaverineTablets |
Each FilmCoated Tablet Contains:
Aceclofenac
Drotaverine Hydrochloride
Excipients
Colour : ApprovedColour Used |
IP
IP |
100mg
80mg
q.s. |
7 |
Aceclofenac & Paracetamol Tablets |
Each Uncoated Tablets Contains:
Aceclofenac
Paracetamol
Excipients
Approved colour used |
IP
IP |
100 mg
325 mg
q.s. |
8 |
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. |
9 |
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. |
10 |
Aceclofenac & Thiocolchicoside Tablets |
Each FilmCoated Tablet Contains:
Aceclofenac
Thiocolchicoside
Excipients
Colour : ApprovedColour Used |
IP
IP |
100mg
4mg
q.s. |
11 |
Aceclofenac & Thiocolchicoside Tablets |
Each FilmCoated Tablet Contains:
Aceclofenac
Thiocolchicoside
Excipients
Colour : ApprovedColour Used |
IP
IP |
100mg
8mg
q.s. |
12 |
Aceclofenac Sustained Release Tablets |
Each FilmCoatedTablet Contains:
Aceclofenac
(AsSustained Release)
Excipients
Colour : ApprovedColour Used |
IP |
200mg
q.s. |
13 |
Aceclofenac Tablets |
Each film coated Tablets Contains :
Aceclofenac
Excipients
Approved colour used. |
IP |
100mg
q.s. |
14 |
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 |
15 |
Aceclofenac, Paracetamol & Chlorzoxazone Tablets |
Each Film coated Tablet Contains:
Aceclofenac
Paracetamol
Chlorzoxazone
Excipients
Approved colour used |
IP
IP
USP |
100mg
325mg
500mg
q.s. |
16 |
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. |
17 |
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. |
18 |
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. |
19 |
Aceclofenac, Paracetamol & Thiocolchicoside Tablet |
Each FilmCoatedTablet Contains
Aceclofenac
Paracetamol
Thiocolchicoside
Excipients
Approved colour used |
IP
IP
q.s. |
100 mg
325 mg
4 mg |
20 |
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. |
21 |
Aceclofenac, Paracetamol Tablets |
Each FilmcoatedTabletsContains:
Aceclofenac
Paracetamol
Excipients
Approved colour used |
IP
IP |
100 mg
325 mg
q.s. |
22 |
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. |
23 |
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. |
24 |
Aciclovir Dispersible Tablet IP |
Each uncoated tablet contains:
Aciclovir
Excipients
Approved colour used |
IP |
800 mg |
25 |
Aciclovir Tablet IP |
Each uncoated tablet contain:
Aciclovir
Excipients
Approved colour used |
IP |
800 mg
q.s. |
26 |
Acyclovir Dispersible Tablets IP |
Each uncoatedTabletsContains:
Acyclovir
Excipients
Approved colour used |
IP |
400 mg
q.s. |
27 |
Albendazole & Ivermectin Tablet |
Each Uncoated tablet contains:
Albendazole
Ivermectin
Excipients
Colour :-Approved colour used |
IP
IP |
400mg
6mg
q.s. |
28 |
Albendazole Tablet IP |
Each Uncoated Chewable Tablet Contains:-
Albendazole
Excipients
Colour:-Approved Colour used |
IP |
400mg
q.s. |
29 |
Allopurinol Tablets IP |
Each uncoated tablets contains:
Allopurinol
Excipients
Approved colour used |
IP |
100 mg
q.s. |
30 |
Allopurinol Tablets IP |
Each uncoated tablets contains:
Allopurinol
Excipients
Approved colour used |
IP |
300 mg
q.s. |
31 |
Alprazolam Tablets IP |
Each uncoated tablet contains:
Alprazolam
Excipients
Approved colour used |
IP |
0.25 mg
q.s |
32 |
Alprazolam Tablets IP |
Each uncoated tablet contains:
Alprazolam
Excipients
Approved colour used |
IP |
0.5 mg
q.s |
33 |
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. |
34 |
Amisulpride Tablets IP |
Each Uncoated Tablet Contains:
Amisulpride
Excipients
Approved colour used. |
IP |
100mg
q.s. |
35 |
Amitriptyline Hydrochloride Tablets IP |
Each film coated tablet contains:-
Amitriptyline Hydrochloride
Excipients
Colour:- Approved Colour used |
IP |
10 mg
q.s |
36 |
Amitriptyline Hydrochloride Tablets IP |
Each film coated tablet contains:-
Amitriptyline Hydrochloride
Excipients
Colour:- Approved Colour used |
IP |
25 mg
q.s. |
37 |
Amitriptyline Hydrochloride Tablets IP |
Each film coated tablet contains:-
Amitriptyline Hydrochloride
Excipients
Colour:- Approved Colour used |
IP |
50 mg
q.s. |
38 |
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. |
39 |
Amlodipine Tablets IP |
Each uncoated tablet contains:-
Amlodipine Besylate
Equivalent to Amlodipine
Excipients
Colour : Approved Coloured Used |
IP |
5 mg
q.s |
40 |
AmlodipineTablets IP |
Each uncoated tablet contains:-
Amlodipine Besylate
Equivalent to Amlodipine
Excipients
Colour : Approved Coloured Used |
IP |
10 mg
q.s |
41 |
AmlodipineTablets IP |
Each uncoated Tablet contains:
Amlodipine Besylate
Equ. to Amlodipine
Excipients
Approved colour used |
IP |
2.5mg
q.s. |
42 |
Artemether & Lumifantrine Tablets |
Each uncoatedTabletsContains:
Artemether
Lumifantrine
Excipients
Approved colour used |
IP |
80 mg
480 mg
q.s. |
43 |
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 |
44 |
Ascorbicacid Tablet IP |
Each Uncoated ChewableTablet Contains
Ascorbic acid
Excipients
Colour : ApprovedColour Used |
IP |
500mg |
45 |
Atenolol Tablets IP |
Each Uncoated Tablet Contains:
Atenolol
Excipients
Colour : Approved Coloured Used |
IP |
50mg
q.s |
46 |
Atenolol Tablets IP |
Each Uncoated Tablet Contains:
Atenolol
Excipients
Colour : Approved Coloured Used |
IP |
100mg
q.s |
47 |
Atorvastatin & FinofibrateTablets |
Each filmcoated tablet contain
Atorvastin Calcium
Eq.to Atorvastin
Finofibrate
Excipients
Approved colour used |
IP
IP |
10 mg
160 mg
q.s. |
48 |
Atorvastatin Tablets IP |
Each film coated tablet contains:-
Atorvastatin Calcium
Eq. toAtorvastatin
Excipients
Colour:-Approved colour used |
IP |
10 mg
q.s. |
49 |
Atorvastatin Tablets IP |
Each film coated tablet contains:-
Atorvastatin Calcium
Eq. toAtorvastatin
Excipients
Colour:-Approved colour used |
IP |
20 mg
q.s. |
50 |
Atorvastatin Tablets IP |
Each film coated tablet contains:-
Atorvastatin Calcium
Eq. toAtorvastatin
Excipients
Colour:-Approved colour used |
IP |
40 mg
q.s. |
51 |
Atorvastatin Tablets IP |
Each film coated tablet contains:-
Atorvastatin Calcium
Eq. toAtorvastatin
Excipients
Colour:-Approved colour used |
IP |
80 mg
q.s. |
52 |
Azathioprine Tablets IP |
Each uncoated tablet contains:
Azathioprine
Excipients
Approved colour used. |
IP |
50mg
q.s. |
53 |
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 |
54 |
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 |
55 |
Azithromycin Dispersible Tablet |
Each uncoated dispersible Tablet Contains :
Azithromycin Dihydrate
Equ. to Azithromycin anhydrous
Excipients
Colour : Approved Coloured Used |
IP |
100mg |
56 |
Azithromycin Tablet IP |
Each film coated tablet contains:
Azithromycin Dihydrate
Equivalent to Azithromycin anhydrous
Excipients
Approved colour used |
IP |
250 mg
q.s. |
57 |
Azithromycin Tablet IP |
Each film coated tablet contains:
Azithromycin Dihydrate
Equivalent to Azithromycin anhydrous
Excipients
Approved colour used |
IP |
500 mg
q.s. |
58 |
Baclofen Tablets IP |
Each uncoated tablet contains:
Baclofen
Excipients
Approved colour used. |
IP |
10mg
q.s. |
59 |
Baclofen Tablets IP |
Each uncoated tablet contains:-
Baclofen
Excipients
Approved colour used. |
IP |
25mg
q.s |
60 |
Betahistine Tablet (SR) IP |
Each uncoated sustainedrelease tablet contain:
Betahistine Hydrochloride
Excipients
Approved colour used |
IP |
24 mg
q.s. |
61 |
Betahistine Tablet IP |
Each Uncoated Tablet Contains:-
Betahistine hydrochloride
Excipients
Approved colour used |
IP |
8mg
q.s |
62 |
Betahistine Tablet IP |
Each Uncoated Tablet Contains:-
Betahistine hydrochloride
Excipients
Approved colour used |
IP |
16 mg
q.s. |
63 |
Betahistine Tablets IP |
Each uncoated tablets contains:
Betahistine Hydrochloride
Excipients
Approved colour used |
IP |
8 mg
q.s. |
64 |
Betahistine Tablets IP |
Each uncoated tablets contains:
Betahistine Hydrochloride
Excipients
Approved colour used |
IP |
16 mg
q.s. |
65 |
Betahistine Tablets IP |
Each uncoated Tablet contains:
Betahistine Hydrochloride
Excipients
Approved colour used. |
IP |
24mg
q.s. |
66 |
Betamethasone Tablets IP |
Each uncoated tablet contains:-
Betamethasone
Excipients
Colour : Approved Coloured Used |
IP |
0.5mg
q.s. |
67 |
Bilastine & Montelukast Tablets |
Each Film Coated bilayered tablet Contains:
Montelukast Sodium eq. to
Montelukast
Bilastine
Excipients
Approved colour used. |
IP |
10mg
20mg
q.s. |
68 |
Bilastine Tablets |
Each Film Coated Tablet Contains:
Bilastine
Excipients
Approved colour used |
|
20mg
q.s. |
69 |
Biotin & FolicAcid Tablets |
Each film coated Tablet contains:
Biotin
Folic Acid
Excipients
Approved Colour used |
USP
IP |
5mg
5mg
q.s |
70 |
Biotin Tablets USP |
Each Film coated Tablet Contains :
Biotin
Excipients
Approved colour used |
USP |
10mg
q.s. |
71 |
Bisacodyl Tablets IP |
Each enteric coated tablet contains:
Bisacodyl
Excipients
Approved colour used |
IP |
5mg
q.s. |
72 |
Bisoprolol Fumarate Tablets |
Each film coated tablet contains:
Bisoprolol Fumarate
Excipients
Approved colour used. |
IP |
2.5mg
q.s. |
73 |
Bisoprolol Fumerate Tablets |
Each film coated tablet contains:
Bisoprolol Fumerate
Excipients
Approved colour used. |
IP |
5mg
q.s. |
74 |
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. |
75 |
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. |
76 |
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. |
77 |
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. |
78 |
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. |
79 |
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. |
80 |
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. |
81 |
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. |
82 |
Calcium Pantothenate Tablets I.P. 200mg |
Each film coated tablet contains:
D-Calcium Pantothenate
Excipients
Approved colour used. |
I.P. |
200mg
q.s. |
83 |
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. |
84 |
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. |
85 |
Carbamazepine Tablets IP |
Each uncoated tablet contains:-
Carbamazepine
Excipients
Colour:- Approved Colour used |
IP |
200 mg
q.s. |
86 |
Carbimazole Tablets IP |
Each Film coated Tablet Contains :
Carbimazole
Excipients
Approved colour used |
IP |
5mg
q.s. |
87 |
Carisoprodol Tablets IP |
Each Uncoated tablet contains:-
Carisoprodol
Excipients
Colour:- Approved Colour used |
IP |
350 mg
q.s |
88 |
Carvedilol Tablets IP |
Each film coated Tablet contains:
Carvedilol
Excipients
Approved colour used |
IP |
3.125mg
q.s. |
89 |
Carvedilol Tablets IP |
Each uncoated Tablet Contains:
Carvedilol
Excipients
Approved colour used |
IP |
12.5mg
q.s. |
90 |
Carvedilol Tablets IP |
Each Uncoated Tablet contains:
Carvedilol
Excipients
Approved colour used |
IP |
6.25mg
q.s. |
91 |
Carvedilol Tablets IP |
Each Uncoated Tablet contains:
Carvedilol
Excipients
Approved colour used |
IP |
3.125mg
q.s. |
92 |
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. |
93 |
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. |
94 |
Cetirizine Hydrochloride Tablets IP |
Each uncoated tablet contains:-
Cetirizine Hydrochloride
Excipients
Colour:- Approved Colour used |
IP |
10 mg
q.s. |
95 |
Chlordiazepoxide & Clidinium Bromide Tablet |
Each FilmCoated tablet contains
Chlordiazepoxide
Clidinium Bromide
Excipients
Approved Colour used |
IP
IP |
5mg
2.5mg
q.s |
96 |
Chlorpheniramine Maleate tablet IP |
Each Uncoated Tablet Contains:
Chlorpheniramine Maleate
Equ. to Chlorpheniramine
Excipients |
IP |
4mg
q.s. |
97 |
Chlorpromazine Hydrochloride Tablets IP |
Each film coated tablet contains:-
Chlorpromazine Hydrochloride
Excipients
Colour:- Approved Colour used |
IP |
50 mg
q.s. |
98 |
Chlorpromazine Hydrochloride Tablets IP |
Each film coated tablet contains:-
Chlorpromazine Hydrochloride
Excipients
Colour:- Approved Colour used |
IP |
100 mg
q.s. |
99 |
Chlorpromazine Hydrochloride Tablets IP |
Each film coated Tablet Contains:
Chlorpromazine Hydrochloride
Excipients
Approved colour used. |
IP |
50mg
q.s. |
100 |
Cholecalciferol Tablet IP |
Each uncoated chewable tablet contains
Cholecalciferol (Stabilized)
Excipients
Colour :- Approved colour used |
IP |
60000IU
q.s. |
101 |
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. |
102 |
Cilnidipine Tablet |
Each film coated tablet contains
Cilnidipine
Excipients
Colour :- Approved Colour Use |
IP |
10mg
q.s |
103 |
Cilnidipine Tablets IP |
Each film coated tablet contains:
Cilnidipine
Excipients
Approved colour used. |
IP |
5mg
q.s. |
104 |
Cilnidipine Tablets IP |
Each film coated tablet contains:
Cilnidipine
Excipients
Approved colour used. |
IP |
5mg
q.s. |
105 |
CilnidipineTablets IP |
Each film coated Tablet contains:
Cilnidipine
Excipients
Approved colour used. |
IP |
20mg
q.s. |
106 |
Cilostazol Tablets IP |
Each uncoated tablet contains:
Cilostazol
Excipients
Approved colour used. |
IP |
50mg
q.s. |
107 |
Cilostazol Tablets IP |
Each uncoated tablet contains:
Cilostazol
Excipients
Approved colour used. |
IP |
100mg
q.s. |
108 |
Cinnarizine (SR)Tablet IP |
Each uncoatedtablet contain:
Cinnarizine
(AsSustained Release)
Excipients
Approved colour used |
IP |
75 mg
q.s. |
109 |
Cinnarizine and Dimenhydrinate Tablets |
Each uncoated Tablet contains:
Cinnarizine
Dimenhydrinate
Excipients
Approved Colour used |
IP
BP |
20mg
40mg
q.s |
110 |
Cinnarizine Tablet IP |
Each uncoated tablet contain:
Cinnarizine
Excipients
Approved colour used |
IP |
25 mg
q.s. |
111 |
Cinnarizine Tablets IP |
Each uncoated Tablet contains
Cinnarizine
Excipients
Approved Coloured used |
IP |
75mg
q.s |
112 |
Cinnarizineand Domperidone Tablets |
Each uncoatedTabletsContains:
Cinnarizine
Domperidone
Excipients
Approved colour used |
IP
IP |
20 mg
15 mg
q.s. |
113 |
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 |
114 |
Ciprofloxacin Tablets IP |
Each film coated tablet contains:-
Ciprofloxacin Hydrochloride
Eq. tociprofloxacin
Excipients
Colour:-Approved colour used |
IP |
250 mg
q.s. |
115 |
Ciprofloxacin Tablets IP |
Each film coated tablet contains:-
Ciprofloxacin Hydrochloride
Eq. tociprofloxacin
Excipients
Colour:-Approved colour used |
IP |
500 mg
q.s. |
116 |
Citicoline & PiracetamTablets |
Each FilmcoatedTabletsContains:
Piracetam
Citicoline sodium
Equivalent toCiticoline
Excipients
Approved colour used |
IP
IP |
800 mg
500 mg
q.s. |
117 |
CiticolineTablets |
Each FilmcoatedTabletsContains:
Citicoline sodium
Equivalent toCiticoline
Excipients
Approved colour used |
IP |
500 mg
q.s. |
118 |
Clarithromycin Tablet IP |
Each film coated tablet Contains:-
Clarithromycin
Excipients
Colour :-Approved colour used |
IP |
250mg
q.s |
119 |
Clarithromycin Tablet IP |
Each film coatedtablet contain:
Clarithromycin
Excipients
Approved colour used |
IP |
500 mg
q.s |
120 |
Clomifene Tablets IP |
Each uncoated tablet contains:
Clomifene Citrate
Excipients
Approved colour used. |
IP |
50mg
q.s. |
121 |
Clomiphene Citrate Tablets IP |
Each Uncoated Tablet Contains:
Clomiphene Citrate
Excipients |
IP |
50mg
q.s. |
122 |
Clomiphene Tablet IP |
Each uncoated Tablet Contains :-
Clomiphene Citrate
Excipients
Colour :- Approved colour used |
IP |
50mg
q.s |
123 |
Clonazepam Tablet IP |
Each uncoated Tablet contains:
Clonazepam
Excipients
Approved colour used |
IP |
0.25mg
q.s |
124 |
Clonazepam Tablet IP |
Each uncoated Tablet contains:
Clonazepam
Excipients
Approved colour used |
IP |
0.5mg
q.s |
125 |
Clopidogrel Bisulphate Tablet |
Each film coated Tablet Contains:
Clopidogrel Bisulphate
Equ. toClopidogrel
Excipients
Colour : Approved Coloured Used |
IP |
75mg
q.s |
126 |
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 |
127 |
Cyproheptadine Hydrochloride Tablet IP |
Each uncoated tablet contains : -
Cyproheptadine Hydrochloride
(as anhydrous)
Excipients
Colour : Approved Colour Used |
IP |
4mg
q.s |
128 |
Cyproheptadine Tablet IP |
Each uncoated tablet contains:
Cyproheptadine Hydrochloride (Anhydrous)
Excipients
Approved colour used |
IP |
4 mg |
129 |
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. |
130 |
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. |
131 |
Dapagliflozin Tablet |
Each film coated tablet contain:
Dapagliflozin propanediol monohydrate
Eq. to Dapagliflozin
Excipients
Approved colour used |
|
10 mg
q.s |
132 |
Dapagliflozin Tablets |
Each film coated tablet contain:
Dapagliflozin propanediol monohydrate
Eq. to Dapagliflozin
Excipients
Approved colour used |
|
5 mg
q.s |
133 |
Dapoxetine Tablets IP |
Each film coated tablet contains:
Dapoxetine Hydrochloride
Equ. to Dapoxetine
Excipients
Approved colour used |
IP |
30 mg
q.s |
134 |
Dapoxetine Tablets IP |
Each film coated tablet contains:
Dapoxetine Hydrochloride
Equ. to Dapoxetine
Excipients
Approved colour used |
IP |
60 mg
q.s |
135 |
Deflazacort Tablets |
Each Uncoated Tablet Contains:
Deflazacort
Excipients
Approved Colour used |
|
18mg
q.s |
136 |
Deflazacort Tablets |
Each uncoated tablet contains:
Deflazacort
Excipients
Colour:- Approved colour used |
IP |
12 mg
q.s. |
137 |
DeflazacortTablet |
Each uncoated tablet contain:
Deflazacort
Excipients
Approved colour used |
|
30 mg
q.s. |
138 |
DeflazacortTablets |
Each uncoated tablet contains:-
Deflazacort
Excipients
Colour:-Approved colour used |
IP |
6 mg
q.s. |
139 |
Desloratadine Tablet |
Each film coated Tablet Contains:-
Desloratadine
Excipients
Approved colour used |
BP |
5 mg
q.s. |
140 |
Dexamethasone Tablets IP |
Each uncoated tablet contains:-
Dexamethasone
Excipients
Colour : Approved Coloured Used |
IP |
0.5 mg
q.s. |
141 |
Dexketoprofen Tablet |
Each film coated Tablet Contains:
Dexketoprofen trometamol
Equ. to Dexketoprofen
Excipients
Colour : Approved Coloured Used |
|
25mg
q.s |
142 |
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. |
143 |
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 |
144 |
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 |
145 |
Diclofenac & TolperisoneTablets |
Each uncoated sustained releaseTablet contains:
Tolperisone Hydrochloride
Diclofenac Sodium
Excipients
Approved colour used |
IP |
450mg
100mg
q.s. |
146 |
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. |
147 |
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. |
148 |
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. |
149 |
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. |
150 |
Diclofenac Potassium & Metaxalone Tablets |
Each uncoated Tablet contains:
Diclofenac Potassium
Metaxalone
Excipients
Approved colour used |
BP |
50mg
400mg
q.s. |
151 |
Diclofenac Potassium & Paracetamol Tablets |
Each film coated Tablet Contains:
Diclofenac Potassium
Paracetamol
Excipients
Approved colour used |
BP
IP |
50mg
325mg
q.s. |
152 |
Diclofenac Potassium & Paracetamol Tablets |
Each film coated Tablet Contains:
Diclofenac Potassium
Paracetamol
Excipients
Approved colour used |
BP
IP |
50mg
325mg
q.s. |
153 |
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. |
154 |
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. |
155 |
Diclofenac Potassium & Thiocolchicoside Tablets |
Each enteric coated tablet contains:
Diclofenac Potassium
Thiocolchiside
Excipients
Approved colour used. |
I.P.
I.P. |
50mg
4mg
q.s. |
156 |
Diclofenac Potassium Sustained Release Tablets |
Each film coated sustainedrelease tablet contains:
Diclofenac Potassium
Excipients
Approved colour used |
BP |
100 mg
q.s. |
157 |
Diclofenac Potassium Tablets IP |
Each Filmcoated Tablet contains:
Diclofenac Potassium
Excipients
Approved colour used |
IP |
25mg
q.s. |
158 |
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. |
159 |
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. |
160 |
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. |
161 |
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. |
162 |
Diclofenac Sodium & Paracetamol Tablets |
Each film coated tablets contains:
Diclofenac Sodium
(as Enteric coated)
Paracetamol
Excipients
Approved colour used |
IP
IP |
50mg
325mg |
163 |
Diclofenac Sodium & Paracetamol Tablets IP |
Each Uncoated Bilayered tablet contains :
Diclofenac Sodium
Paracetamol
Excipients
Approved colour used. |
IP
IP |
50mg
325mg
q.s. |
164 |
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. |
165 |
Diclofenac Sodium SR Tablet IP |
Each film coated Sustained Release tablet Contains
Diclofenac Sodium
Excipients
Colour :-Approved colour used |
IP |
100mg
q.s |
166 |
Diclofenac Sodium Tablets IP |
Each Enteric Coated Tablet Contains:
Diclofenac Sodium
Excipients
Approved Colour Used |
IP |
50mg
q.s |
167 |
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. |
168 |
Dicyclomine Hydrochloride& Paracetamol Tablets |
Each uncoated Tablet contains:
Dicyclomine Hydrochloride
Paracetamol
Excipients
Approved colour used |
IP
IP |
20mg
500mg
q.s. |
169 |
Digoxin Tablets IP |
Each Uncoated Tablet Contains:
Digoxin
Excipients |
IP |
0.25mg
q.s. |
170 |
Digoxin Tablets IP |
Each uncoated Tablet Contains:
Digoxin
Excipients
Approved colour used |
IP |
0.25mg
q.s. |
171 |
Disulfiram Tablets |
Each Uncoated Tablet Contains:-
Disulfiram
Excipients
Colour :- Approved colour used |
IP |
200mg
q.s |
172 |
Domperidone DispersibleTablets |
Each uncoated dispersible tablet contains:
Domperidone
Excipients
Approved colour used |
IP |
10mg
q.s |
173 |
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. |
174 |
Doxofylline & Ambroxol Hydrochloride Tablets |
Each Film coated Tablet Contains :
Doxofylline
Ambroxol Hydrochloride
Excipients
Approved colour used |
IP
IP |
400mg
30mg
q.s. |
175 |
Doxofylline Modified Release Tablets |
Each uncoated Modified Release Tablet contains :
Doxofylline
Excipients |
IP |
650mg
q.s. |
176 |
Doxofylline Tablets IP |
Each filmCoatedTablet Contains:-
Doxofylline
Excipients
Colour :-Approved colour used |
IP |
400mg
q.s. |
177 |
Doxofylline Tablets IP |
Each uncoated Tablet Contains :-
Doxofylline
Excipients |
IP |
400mg
q.s. |
178 |
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. |
179 |
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. |
180 |
Doxycycline Hyclate Tablets |
Each film coated Tablet Contains:
Doxycycline Hyclate
Equ. to Doxycycline
Excipients
Approved colour used. |
IP |
100mg
q.s. |
181 |
Doxylamine Succinate & Pyridoxine HCl Tablets |
Each enteric coated tablet contains :
Doxylamine Succinate
Pyridoxine Hydrochloride
Excipients
Approved colour used |
USP
IP |
10mg
10mg
q.s |
182 |
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. |
183 |
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. |
184 |
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 |
185 |
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. |
186 |
Drotaverine Hydrochloride Tablet IP |
Each film coated tablet Contains:-
Drotaverine Hydrochloride
Excipients
Colour :-Approved colour used |
IP |
40mg
q.s. |
187 |
Drotaverine Hydrochloride Tablets IP |
Each uncoated Tablet contains
Drotaverine Hydrochloride
Excipients
Approved Coloured used |
IP |
80mg
q.s |
188 |
Drotaverine Hydrochloride Tablets IP |
Each Film coated Tablet contains
Drotaverine Hydrochloride
Excipients
Colour : Approved Coloured used |
IP |
80mg
q.s |
189 |
Duloxetine Gastro- resistant Tablets IP |
Each enteric coated Tablet contains :
Duloxetine Hydrochloride
Equ. to Duloxetine
Excipients
Approved Colour used. |
IP |
20mg
q.s. |
190 |
EbastineTablet IP |
Each film coated tablet contains:
Ebastine
Excipients
Approved colour used |
IP |
10 mg
q.s |
191 |
EbastineTablet IP |
Each film coated tablet contains:
Ebastine
Excipients
Approved colour used |
IP |
20 mg
q.s |
192 |
Empagliflozin & Linagliptin Tablets |
Each film coated tablet contains:-
Empagliflozin
Linagliptin
Excipients
Approved colour used . |
|
10mg
5mg
q.s. |
193 |
Empagliflozin & Linagliptin Tablets |
Each film coated tablet contains:-
Empagliflozin
Linagliptin
Excipients
Approved colour used . |
|
25mg
5mg
q.s. |
194 |
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 |
195 |
Erythromycin StearateTablet IP |
Each film coated Tablet Contains:
Erythromycin Stearate
Equ. toErythromycin
Excipients
Colour:- Approved colour used |
IP |
250mg |
196 |
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. |
197 |
Escitalopram Oxalate Tablet |
Each film coated Tablet Contains:
Escitalopram oxalate
Equ. toEscitalopram
Excipients
Colour : Approved Coloured Used |
IP |
10mg
q.s |
198 |
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. |
199 |
Etizolam Tablets |
Each film coated tablet contains:
Etizolam
Excipients
Approved colour used |
|
0.25 mg
q.s |
200 |
Etizolam Tablets |
Each film coated tablet contains:
Etizolam
Excipients
Approved colour used |
|
0.5 mg
q.s |
201 |
Etodolac Extended Release Tablets USP |
Each Film Coated Extended Release Tablet contains :
Etodolac
Excipients
Approved colour used |
IP |
600mg
q.s. |
202 |
Etodolac Tablets IP |
Each Film Coated Tablet contains:
Etodolac
Excipients
Approved colour used |
IP |
400mg
q.s. |
203 |
Etodolac Tablets IP |
Each Film Coated Tablet contains:
Etodolac
Excipients
Approved colour used |
IP |
300mg
q.s. |
204 |
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 |
205 |
Etoricoxib & Paracetamol Tablets |
Each film coated tablet Contains:-
Etoricoxib
Paracetamol
Excipients
Colour :-Approved colour used |
IP
IP |
60mg
325mg
q.s |
206 |
Etoricoxib & Thiocolchicoside Tablets |
Each film coated tablet Contains:-
Etoricoxib
Thiocolchicoside
Excipients
Colour :-Approved colour used |
IP
IP |
60mg
4mg
q.s |
207 |
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. |
208 |
Etoricoxib tablets IP |
Each film coated tablet contains:-
Etoricoxib
Excipients
Colour:-Approved Colour Used |
IP |
90 mg
q.s. |
209 |
Etoricoxib tablets IP |
Each film coated tablet contains:-
Etoricoxib
Excipients
Colour:-Approved Colour Used |
IP |
60 mg
q.s. |
210 |
Etoricoxib tablets IP |
Each film coated tablet contains:-
Etoricoxib
Excipients
Colour:- Approved Colour Used |
IP |
120 mg
q.s. |
211 |
Febuxostat Tablet |
Each film coated tablet contains:
Febuxostat
Excipients
Approved colour used |
|
120 mg
q.s |
212 |
FebuxostatTablets |
Each film coated tablet contains:-
Febuxostat
Excipients
Colour:-Approved colour used |
|
40 mg
q.s. |
213 |
FebuxostatTablets |
Each film coated tablet contains:-
Febuxostat
Excipients
Colour:-Approved colour used |
|
80 mg
q.s. |
214 |
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. |
215 |
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. |
216 |
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 |
217 |
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. |
218 |
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 |
219 |
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 |
220 |
Fexofenadine & Montelukast ChewableTablets |
Each Uncoated Chewable Tablet Contains :
Fexofenadine Hydrochloride
Montelukast Sodium
Equ. to Montelukast
Excipients |
IP
IP |
120mg
10mg
q.s. |
221 |
Fexofenadine & MontelukastTablet |
Each uncoatedTablet contains
Fexofenadine Hydrochloride
Equ. to Fexofenadine
Montelukast Sodium
Equ. toMontelukast
Excipients
Colour : ApprovedColour Used |
IP
IP |
120mg
10mg
q.s. |
222 |
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. |
223 |
Fexofenadine Hydrochloride Tablet IP |
Each uncoatedTablet contains
Fexofenadine Hydrochloride
Equ. to Fexofenadine
Excipients
Colour : ApprovedColour Used |
IP |
120mg
q.s |
224 |
Fexofenadine Hydrochloride Tablets IP |
Each FilmcoatedTabletsContains:
Fexofenadine Hydrochloride
Excipients
Approved colour used |
IP |
180 mg
q.s. |
225 |
Fexofenadine Hydrochloride Tablets IP |
Each film coated tablet contains:
Fexofenadine Hydrochloride
Excipients
Approved colour used. |
IP |
120mg
q.s |
226 |
Flavoxate Tablet IP |
Each film coated tablet contains:
Flavoxate
Excipients
Approved colour used |
IP |
200 mg
q.s |
227 |
Fluconazole Tablet IP |
Each Uncoated Tablet Contains: -
Fluconazole
Excipients
Colour : -ApprovedColour used |
IP |
150mg
q.s. |
228 |
Fluconazole Tablets IP |
Each uncoated tablet Contains:
Fluconazole
Excipients
Approved colour used |
IP |
400mg
q.s. |
229 |
FluconazoleTablets IP |
Each uncoated tablets contains:
Fluconazole
Excipients
Approved colour used |
IP |
200 mg
q.s. |
230 |
Flunarizine Tablets |
Each Uncoated Tablet Contains:
Flunarizine
(as Flunarizine Dihydrochloride)
Excipients
Approved colour used |
BP |
5mg
q.s. |
231 |
Flunarizine Tablets IP |
Each uncoated Tablet contains
Flunarizine Hydrochloride
Excipients
Approved Coloured used |
BP |
10mg
q.s |
232 |
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 |
233 |
FluoxetineTablet IP |
Each film coated tablet Contains:-
Fluoxetine Hydrochloride
Equ. toFluoxetine
Excipients
Colour :-Approved colour used |
IP |
20mg
q.s. |
234 |
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 |
235 |
Folic Acid Tablets IP |
Each uncoated Tablet Contains:
Folic Acid
Excipients
Approved Colour used |
IP |
5mg
q.s |
236 |
Folic Acid Tablets IP |
Each uncoated Tablet Contains:
Folic Acid
Excipients
Approved Colour used |
IP |
10mg
q.s |
237 |
Frusemide Tablets IP |
Each uncoated tablet contains:
Frusemide
Excipients
Approved colour used. |
IP |
40mg
q.s. |
238 |
Furosemide Tablets IP |
Each Uncoated Tablet Contains:
Furosemide
Excipients |
IP |
40mg
q.s. |
239 |
Gabapentin & Methylcobalamin Tablet |
Each film coated tablet contains;
Gabapentin
Methylcobalamine
Excipients
Approved colour used |
IP
IP |
300mg
500mcg
q.s |
240 |
Gabapentin & Methylcobalamin Tablets |
Each film coated Tablet Contains:
Gabapentin
Methylcobalamin
Excipients
Approved colour used. |
IP
IP |
100mg
500mcg
q.s. |
241 |
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 |
242 |
Gabapentin Tablet IP |
Each film coated tablet contains:
Gabapentin
Excipients
Approved colour used |
IP |
100 mg
q.s |
243 |
Gabapentin Tablet IP |
Each film coated tablet contains:
Gabapentin
Excipients
Approved colour used |
IP |
400 mg
q.s |
244 |
Gabapentin Tablet IP |
Each film coated tablet contains:
Gabapentin
Excipients
Approved colour used |
IP |
800 mg
q.s |
245 |
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. |
246 |
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. |
247 |
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. |
248 |
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. |
249 |
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. |
250 |
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. |
251 |
GlimepirideTablet IP |
Each uncoated tablet contains:
Glimepiride
Excipients
Approved colour used |
IP |
1 mg
q.s. |
252 |
GlimepirideTablet IP |
Each uncoated tablet contains:
Glimepiride
Excipients
Approved colour used |
IP |
2 mg
q.s. |
253 |
Griseofulvin Tablets IP |
Each uncoated Tablet Contains:
Griseofulvin
Excipients
Approved Colour Used |
IP |
250mg
q.s |
254 |
Griseofulvin Tablets IP |
Each Uncoated Tablet Contains:
Griseofulvin
Excipients |
IP |
500mg
q.s. |
255 |
Haloperidol Tablet IP |
Each Uncoated Tablet Contains:
Haloperidol
Excipients |
IP |
5mg
q.s. |
256 |
Hydoxychloroquine Tablets IP |
Each film coatedtablets contain:
Hydroxychloroquine Sulphate
Excipients |
IP |
200 mg
q.s. |
257 |
Hydoxychloroquine Tablets IP |
Each film coatedtablets contain:
Hydroxychloroquine Sulphate
Excipients |
IP |
400 mg
q.s. |
258 |
Hydrochlorothiazid e tablet IP |
Each film coated tablet contains:-
Hydrochlorothiazide
Excipients
Colour : Approved Colour Used |
IP |
25mg
q.s |
259 |
Hydrochlorothiazid e tablet IP |
Each film coated tablet contains:-
Hydrochlorothiazide
Excipients
Colour : Approved Colour Used |
IP |
50mg
q.s |
260 |
Hydroxyzine Hydrochloride Tablet |
Each uncoated tablet contains
Hydroxyzine Hydrochloride
eq. to Hydroxyzine
Excipients
Colour :- Approved Colour Used |
IP |
10mg
q.s. |
261 |
Hydroxyzine Hydrochloride Tablet |
Each uncoated tablet contains
Hydroxyzine Hydrochloride
eq. to Hydroxyzine
Excipients
Colour :- Approved Colour Used |
IP |
25mg
q.s. |
262 |
Hydroxyzine Hydrochloride Tablets IP |
Each Film Coated Tablet Contains:
Hydroxyzine Hydrochloride
Excipients
Approved colour used. |
IP |
25mg
q.s |
263 |
Hyoscine Butylbromide IP |
Each Film coated Tablet Contains :
Hyoscine Butylbromide
Excipients
Approved colour used. |
IP |
10mg
q.s. |
264 |
Ibuprofen & Paracetamol Tablets |
Each uncoated Tablet Contains
Ibuprofen
Paracetamol
Excipients
Approved Colour Used |
IP
IP |
400mg
325mg
q.s |
265 |
Ibuprofen Tablets IP |
Each film coated Tablet contains:
Ibuprofen
Excipients
Approved colour used |
IP |
200mg |
266 |
Ibuprofen Tablets IP |
Each film coated Tablet contains:
Ibuprofen
Excipients
Approved colour used |
IP |
400mg |
267 |
Isosorbide Dinitrate Tablets IP |
Each Uncoated Tablet Contains:
Isosorbide Dinitrate
Excipients
Approved colour used |
IP |
5mg
q.s. |
268 |
Isoxsuprine Tablets (Sustained Release) |
Each uncoated Sustained Release Tablet Contains
Isoxsuprine Hydrochloride
Excipients
Approved colour used |
IP |
40mg
q.s |
269 |
Ivermactin Tablet IP |
Each uncoated tablet contains:
Ivermactin
Excipients
Approved colour used |
IP |
6 mg
q.s |
270 |
Ivermactin Tablet IP |
Each uncoated tablet contains:
Ivermactin
Excipients
Approved colour used |
IP |
12 mg
q.s |
271 |
Ivermectin & Albendazole Tablets |
Each uncoated tablet contains:
Ivermactin
Albendazole
Excipients
Approved colour used |
IP
IP |
12 mg
400mg
q.s |
272 |
Ketoconazole Tablet IP |
Each uncoated tablet contain:
Ketoconazole
Excipients
Approved colour used |
IP |
200 mg
q.s |
273 |
Ketrolac Tromethamine DispersibleTablets |
Each uncoated dispersible tablets contains:
Ketrolac Tromethamine
Excipients
Approved colour used |
IP |
10 mg
q.s. |
274 |
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. |
275 |
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. |
276 |
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. |
277 |
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. |
278 |
Labetalol Tablets IP |
Each film coated Tablet Contains:
Labetalol Hydrochloride
Excipients
Approved colour used. |
IP |
50mg
q.s |
279 |
Labetalol Tablets IP |
Each film coated Tablet Contains:
Labetalol Hydrochloride
Excipients
Approved colour used. |
IP |
100mg
q.s |
280 |
Lansoprazole orally Disintegrating Tablets |
Each uncoated tablet contains:
Lansoprazole
(as enteric coated pellets)
Excipients
Approved colour used |
IP |
15 mg
q.s. |
281 |
Lansoprazole Orally Disintegrating Tablets 30mg |
Each uncoated orallyDisintegrating tablet contains:
Lansoprazole
(As enteric coated pellets)
Excipients
Approved colour used. |
IP |
30mg
q.s. |
282 |
Leflunomide Tablet IP |
Each film coated Tablet Contains:
Leflunomide
Excipients
Colour : Approved Coloured Used |
IP |
20mg
q.s |
283 |
Leflunomide Tablet IP |
Each film coated Tablet Contains:
Leflunomide
Excipients
Colour : Approved Coloured Used |
IP |
10mg
q.s |
284 |
Letrozole Tablets USP |
Each film coated Tablet contains:
Letrozole
Excipients
Approved colour used. |
USP |
2.5mg
q.s. |
285 |
Levetiracetam Tablet IP |
Each film Coated Tablet Contains :-
Levetiracetam
Excipients
Colour :- Approved colour used |
IP |
250mg
q.s |
286 |
Levetiracetam Tablet IP |
Each film Coated Tablet Contains :-
Levetiracetam
Excipients
Colour :- Approved colour used |
IP |
500mg
q.s |
287 |
Levocetirizine Dihydrochloride & Montelukast DispersibleTablets |
Each uncoated dispersible Tablet contains :
Levocetirizine Dihydrochloride
Montelukast sodium
Equ. to Montelukast
Excipients |
IP
IP |
2.5mg
4mg
q.s |
288 |
Levocetirizine Dihydrochloride Tablets IP |
Each Uncoated Tablet Contains:-
Levocetirizine Dihydrochloride
Excipients
Colour :-Approved colour used |
IP |
5mg
q.s. |
289 |
Levocetirizine Dihydrochloride Tablets IP |
Each film Coated Tablet Contains :
Levocetirizine Dihydrochloride
Excipients
Approved colour used. |
IP |
5mg
q.s. |
290 |
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. |
291 |
Levocetirizine Hydrochloride & Ambroxol Hydrochloride Tablet |
Each film coated Tablet contains:
Levocetirizine Hydrochloride
Ambroxol Hydrochloride
Excipients
Approved colour used. |
IP
IP |
5mg
60mg
q.s. |
292 |
Levocetirizine Hydrochloride Tablets IP |
Each Film coated Tablet Contains :
Levocetirizine Hydrochloride
Excipients
Approved colour Used. |
IP |
10mg
q.s. |
293 |
Levodopa & Carbidopa Tablets IP |
Each Uncoated Tablet Contains:
Carbidopa
Equ.ToCarbidopa
AnhydrousLevodopa
Excipients
Approved colour used |
IP
IP |
25mg
250mg
q.s. |
294 |
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. |
295 |
Levofloxacin Tablets IP |
Each film coated tablet contains:-
Levofloxacin Hemihydrate
Equivalent to Levofloxacin
Excipients
Colour:-Approved colour used |
IP |
250 mg.
q.s. |
296 |
Levofloxacin Tablets IP |
Each film coated tablet contains:-
Levofloxacin Hemihydrate
Equivalent to Levofloxacin
Excipients
Colour:-Approved colour used |
IP |
500 mg.
q.s. |
297 |
Levofloxacin Tablets IP |
Each film coated tablet contains:-
Levofloxacin Hemihydrate
Equivalent to Levofloxacin
Excipients
Colour:-Approved colour used |
IP |
750 mg.
q.s. |
298 |
Levosulpiride Tablets |
Each Uncoated Tablet Contains:
Levosulpiride
Excipients |
|
25mg
q.s. |
299 |
Levothyroxine sodium Tablets USP |
Each uncoated Tablet Contains:
Levothyroxine Sodium
Equ. to Anhydrous Levothyroxine Sodium
Excipients |
USP |
50mcg
q.s. |
300 |
LinezolidTablet IP |
Each film coated tablet contains:-
Linezolid
Excipients
Colour:-Approved colour used |
IP |
600 mg
q.s. |
301 |
Lithium Carbonate Prolonged – Release Tablets IP |
Each uncoated Prolonged-Release tablet contains:
Lithium Carbonate
Excipients
Approved colour used. |
IP |
450mg
q.s. |
302 |
Loperamide Hydrochloride Tablets IP |
Each uncoated tablet contains:-
Loperamide Hydrochloride
Excipients
Colour : Approved Coloured Used |
IP |
2 mg
q.s. |
303 |
Loratadine Tablet USP |
Each uncoated table contains:-
Loratadine
Excipients
Approved colour used |
USP |
10 mg
q.s. |
304 |
Lornoxicam & Paracetamol Tablets |
Each film coatedTablet Contains:-
Lornoxicam
Paracetamol
Excipients
Colour :-Approved colour used |
IP
IP |
4mg
325mg
q.s. |
305 |
Lornoxicam & Paracetamol Tablets |
Each film coatedTablet Contains:-
Lornoxicam
Paracetamol
Excipients
Colour :-Approved colour used |
IP
IP |
8mg
325mg
q.s. |
306 |
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. |
307 |
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. |
308 |
Losartan Potassium Tablet IP |
Each film coated tablet contains:
Losartan Potassium
Excipients
Approved colour used |
IP |
50 mg |
309 |
Losartan potassium Tablets IP |
Each film coated tablet contains:
Losartan potassium
Excipients
Approved colour used. |
IP |
25mg
q.s |
310 |
Mecobalamin Tablets |
Each film coated Tablet contains:
Mecobalamin
Excipients
Approved colour used. |
IP |
1500mcg
q.s. |
311 |
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. |
312 |
Mefenamic Acid & Dicyclomine HCl Tablets |
Each uncoated Tablet contains:
Mefenamic Acid
Dicyclomine HCl
Excipients |
IP
IP |
250mg
20mg
q.s |
313 |
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. |
314 |
Mefenamic Acid & Paracetamol Tablet |
Each uncoated tablet contain:
Mefenamic Acid
Paracetamol
Excipients
Approved colour used |
IP
IP |
500 mg
325 mg
q.s. |
315 |
Mefenamic Acid & Paracetamol Tablets |
Each uncoated tablet contains:
Mefenamic Acid
Paracetamol
Excipients
Approved Colour used |
IP
IP |
250mg
325mg
q.s. |
316 |
Memantine Hydrochloride & Donepezil Hydrochloride Tablets |
Each film coated tablet contains:
Memantine Hydrochloride
Donepezil Hydrochloride
Excipients
Approved colour used. |
IP
IP |
5mg
5mg
q.s. |
317 |
Mesalamine Prolonged-release Tablets IP |
Each enteric coated Prolonged-release tablet contains:-
Mesalamine
Excipients
Approved colour used . |
IP |
1200mg
q.s. |
318 |
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. |
319 |
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. |
320 |
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. |
321 |
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. |
322 |
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. |
323 |
Metformin Hydrochloride & GliclazideTablets |
Each uncoated tablets contains:
Metformin hydrochloride
Gliclazide
Excipients
Approved colour used |
IP
IP |
500 mg
80 mg |
324 |
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 |
325 |
Metformin Hydrochloride Sustained-Release Tablets |
Each uncoated Sustained Release Tablet Contains :
Metformin Hydrochloride
Excipients |
IP |
500mg
q.s. |
326 |
Metformin Hydrochloride Sustained-Release Tablets |
Each uncoated Sustained Release Tablet Contains :
Metformin Hydrochloride
Excipients |
IP |
850mg
q.s. |
327 |
Metformin Hydrochloride Sustained-Release Tablets |
Each uncoated Sustained Release Tablet Contains :
Metformin Hydrochloride
Excipients |
IP |
1000mg
q.s. |
328 |
Metformin Hydrochloride Tablets IP |
Each uncoated sustainedrelease tablet contains:
Metformin Hydrochloride
Excipients
Approved colour used |
IP |
500 mg
q.s. |
329 |
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 |
330 |
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 |
331 |
Methotrexate Tablets IP |
Each uncoated tablet contains:
Methotrexate
Excipients
Approved colour used. |
IP |
2.5mg
q.s. |
332 |
Methylcobalamin Sublingual Tablets |
Each uncoated sublingual tablet contains :
Methylcobalamin
Excipients |
IP |
1500mcg
q.s. |
333 |
Methylcobalamin Tablets |
Each film coated Tablet Contains:
Methylcobalamin
Excipients
Approved colour used. |
|
1500mcg
q.s. |
334 |
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. |
335 |
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. |
336 |
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 |
337 |
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. |
338 |
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. |
339 |
Methylprednisolone Tablets |
Each uncoated tablet contains:-
Methylprednisolone
Excipients
Colour :- Approved Colour Used |
IP |
8 mg
q.s. |
340 |
Methylprednisolone Tablets IP |
Each uncoated tablet contains:-
Methylprednisolone
Excipients
Colour :- Approved Colour Used |
IP |
4 mg
q.s. |
341 |
Methylprednisolone Tablets IP |
Each uncoated tablet contains:-
Methylprednisolone
Excipients
Colour :- Approved Colour Used |
IP |
2 mg
q.s. |
342 |
Methylprednisolone Tablets IP |
Each uncoated tablet contains:-
Methylprednisolone
Excipients
Colour :- Approved Colour Used |
IP |
16 mg
q.s. |
343 |
Methylprednisolone Tablets IP |
Each uncoated tablet contains:-
Methylprednisolone
Excipients
Colour :- Approved Colour Used |
IP |
16 mg
q.s. |
344 |
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. |
345 |
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. |
346 |
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. |
347 |
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 |
348 |
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. |
349 |
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. |
350 |
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. |
351 |
Metronidazole Tablet IP |
Each film coated Tablet Contains:
Metronidazole
Excipients
Colour : Approved Coloured Used |
IP |
200mg
q.s |
352 |
Metronidazole Tablet IP |
Each film coated Tablet Contains:
Metronidazole
Excipients
Colour : Approved Coloured Used |
IP |
400mg
q.s |
353 |
Minocycline Hydrochloride Tablet |
Each film coated Tablet Contains
Minocycline Hydrochloride
Equ. to Minocycline
Excipients
Colour : Approved Coloured Used |
USP |
100mg
q.s |
354 |
Minoxidil Tablets IP |
Each Uncoated Tablet Contains:
Minoxidil
Excipients |
IP |
5mg
q.s. |
355 |
Minoxidil Tablets IP |
Each uncoated tablet Contains:
Minoxidil
Excipients
Approved colour used |
IP |
2.5mg
q.s. |
356 |
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 |
357 |
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 |
358 |
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. |
359 |
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. |
360 |
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 |
361 |
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. |
362 |
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. |
363 |
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 |
364 |
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. |
365 |
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 |
366 |
Montelukast Sodium Chewable Tablets |
Each UncoatedChewableTablet Contains:
Montelukast sodium
Equ. To
Montelukast
Excipients |
IP |
4mg
q.s. |
367 |
Montelukast Sodium Tablets IP |
Each Film coated Tablet Contains :
Montelukast Sodium
Equ. to Montelukast
Excipients
Approved colour used |
IP |
10mg
q.s. |
368 |
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 |
369 |
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. |
370 |
Moxifloxacin Hydrochloride Tablets |
Each Film coated Tablet Contains:
Moxifloxacin Hydrochloride
Equ. To
Moxifloxacin
Excipients
Approved colour used. |
IP |
400mg
q.s |
371 |
Moxonidine Tablets |
Each film coated tablet contains:
Moxonidine
Excipients
Approved colour used |
BP |
0.2mg
q.s. |
372 |
Moxonidine Tablets |
Each film coated tablet contains:
Moxonidine
Excipients
Approved colour used |
BP |
0.3mg
q.s. |
373 |
Naproxen & Domperidone Tablets |
Each film coated tablet contains:
Naproxen
Domperidone
Excipients
Approved colour used |
IP
IP |
500mg
10mg
q.s |
374 |
Naproxen & Domperidone Tablets |
Each Film coatedtablet contains:
Naproxen
Domperidone
Excipients
Approved colour used. |
IP
IP |
250 mg
10 mg
q.s |
375 |
Naproxen Sodium & Domperidone Tablet |
Each uncoated tablet contain:
Naproxen Sodium
Domperidone
Excipients
Approved colour used |
IP
IP |
250 mg
10 mg
q.s |
376 |
Naproxen Sustained Release Tablets IP |
Each uncoated sustained release tablet contains:
Naproxen
Excipients
Approved colour used |
IP |
750mg
q.s. |
377 |
Naproxen Tablet IP |
Each uncoated tablet contain:
Naproxen
Excipients
Approved colour used |
IP |
250 mg
q.s |
378 |
Naproxen Tablet IP |
Each uncoated tablet contain:
Naproxen
Excipients
Approved colour used |
IP |
500 mg
q.s |
379 |
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. |
380 |
Nebivolol Hydrochloride Tablets IP |
Each uncoated tablet contains:
Nebivolol Hydrochloride
Eq. to Nebivolol
Excipients
Approved colour used. |
IP |
5mg
q.s. |
381 |
Nicorandil Tablets IP |
Each uncoated Tablets Contains:
Nicorandil
Excipients |
IP |
5mg |
382 |
Nicorandil Tablets IP |
Each uncoated Tablets Contains:
Nicorandil
Excipients |
IP |
10mg |
383 |
Nifedipine Prolonged Release Tablets BP |
Each Prolonged Release film coated tablet contains:
Nifedipine
Excipients
Approved colour used. |
BP |
30mg
q.s. |
384 |
Nimesulide & Paracetamol Tablets |
Each uncoated tablet contains:
Nimesulide
Paracetamol
Excipients |
BP
IP |
20 mg
q.s. |
385 |
Nimesulide & Paracetamol Tablets |
Each uncoated Bilayered Tablet contains:
Nimesulide
Paracetamol
Excipients
Approved colour used. |
BP
IP |
100mg
325mg
q.s. |
386 |
Nimesulide Mouth Dissolving Tablets |
Each uncoated Mouth dissolving Tablet contains :
Nimesulide
Excipients
Approved colour used. |
BP |
100mg
q.s. |
387 |
Nimesulide Tablets |
Each uncoated tablet contains:-
Nimesulide
Excipients
Colour:-Approved colour used |
BP |
100 mg
q.s |
388 |
Nimesulide, Paracetamol & Chlorzoxazone Tablets |
Each film coated tablet contains:
Nimesulide
Paracetamol
Chlorzoxazone
Excipients
Approved colour used |
BP
IP
USP |
100mg
325mg
250mg
q.s |
389 |
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. |
390 |
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 |
391 |
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. |
392 |
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. |
393 |
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. |
394 |
Nimodipine Tablets |
Each Film coated Tablet Contains :
Nimodipine
Excipients
Approved colour used. |
IP |
30mg
q.s. |
395 |
Nitrofurantoin SR Tablet |
Each FilmCoated Sustained ReleaseTablet Contains
Nitrofurantoin
Excipients
Colour :-Approved colour used |
BP |
100mg
q.s. |
396 |
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. |
397 |
Norfloxacin & TinidazoleTablets |
Each film coated tablet contains:-
Norfloxacin
Tinidazole
Excipients
Colour:-Approved colour used |
IP
IP |
400 mg
600 mg
q.s. |
398 |
Norfloxacin Tablets IP |
Each film coated Tablet Contains:
Norfloxacin
Excipients
Approved Colour Use |
IP |
400mg
q.s |
399 |
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. |
400 |
Nortriptyline & PregabalineTablets |
Each film coatedTablet Contains:
Nortriptyline Hydrochloride
Equivalent to Nortriptyline
Pregabaline
Excipients
Approved colour used |
IP
IP |
10 mg
75 mg
q.s. |
401 |
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. |
402 |
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. |
403 |
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. |
404 |
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. |
405 |
Ofloxacin & Ornidazole Tablet IP |
Each FilmCoatedTabletContains:
Ofloxacin
Ornidazole
Excipients
Approved colour used |
IP
IP
q.s. |
200 mg
500 mg |
406 |
Ofloxacin & TinidazoleTablets |
Each film coated tablet contains:
Ofloxacin
Tinidazole
Excipients
Approved colour used. |
IP
IP |
200mg
600mg
q.s. |
407 |
Ofloxacin Tablet IP |
Each film coated tablet contains:-
Ofloxacin
Excipients
Approved colour used |
IP |
400 mg
q.s. |
408 |
Ofloxacin Tablets IP |
Each film coated tablet contains:-
Ofloxacin
Excipients
Colour:-Approved colour used |
IP |
200 mg
q.s. |
409 |
OlanzapineTablet IP |
Each film coated tablet contains:
Olanzapine
Excipients
Approved colour used |
IP |
5mg
q.s. |
410 |
OlanzapineTablet IP |
Each film coated tablet contains:
Olanzapine
Excipients
Approved colour used |
IP |
2.5mg
q.s. |
411 |
OlanzapineTablet IP |
Each film coated tablet contains:
Olanzapine
Excipients
Approved colour used |
IP |
7.5 mg
q.s. |
412 |
OlanzapineTablets IP |
Each film coated tablet contains:
Olanzapine
Excipients
Approved colour used |
IP |
10 mg
q.s. |
413 |
Olmesartan & AmlodipineTablets |
|
IP
IP |
20 mg
5 mg
q.s |
414 |
Olmesartan & Chlorthalidone Tablets |
Each film coated tablet contains:
Olmesartan Medoxomil
Chlorthalidone
Excipients
Approved colour used |
IP
IP |
20 mg
12.5 mg
q.s |
415 |
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 |
416 |
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 |
417 |
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. |
418 |
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 |
419 |
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. |
420 |
Olmesarton Medoxomil Tablet IP |
Each film coated tablet contains:
Olmesarton Medoxomil
Excipients
Approved colour used |
IP |
20 mg
q.s. |
421 |
Olmesarton Medoxomil Tablet IP |
Each film coated tablet contains:
Olmesarton Medoxomil
Excipients
Approved colour used |
IP |
40 mg
q.s. |
422 |
Ondansetron Orally Disintegrating TabletsTablet IP |
Each Uncoated OrallyDisintegrating Tablets Contains
Ondansetron hydrochloride
Equ. toOndansetron
Excipients
Approved colour used. |
IP |
4mg |
423 |
Ondansetron Orally Disintegrating TabletsTablet IP |
Each Uncoated OrallyDisintegrating Tablets Contains
Ondansetron hydrochloride
Equ. toOndansetron
Excipients
Approved colour used |
IP |
8mg |
424 |
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. |
425 |
Ornidazole Tablets |
Each Film coated Tablet Contains :
Ornidazole
Excipients
Approved colour used. |
IP |
500mg
q.s. |
426 |
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. |
427 |
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. |
428 |
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. |
429 |
Pantoprazole Tablets IP |
Each enteric coated Tablet contains :
Pantoprazole sodium sesquihydrate
Equ. to Pantoprazole
Excipients
Approved colour used |
IP |
20mg
q.s. |
430 |
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. |
431 |
Paracetamol (DT) Tablets BP |
Each uncoated dispersible tablet contains:
Paracetamol
Excipients
Approved colour used. |
IP |
650 mg
q.s. |
432 |
Paracetamol & Diclofenac Tablets IP |
Each uncoated tablet contains:-
Paracetamol
Diclofenac Sodium
Excipients
Colour:-Approved colour used |
IP
IP |
325 mg
50 mg
q.s. |
433 |
Paracetamol & Dicyclomine Hydrochloride Tablets |
Each uncoated Tablet contains:
Paracetamol
Dicyclomine Hydrochloride
Excipients |
IP
IP |
325mg
20mg
q.s. |
434 |
Paracetamol & Domperidone Tablets |
Each uncoatedtablet contains :
Paracetamol
Domperidone
Excipients
Approved colour used. |
IP
IP |
325mg
10mg
q.s. |
435 |
Paracetamol and CaffeineTablets IP |
Each uncoated Tablet contains:
Paracetamol
Caffeine
Excipients |
IP
IP |
650mg
50mg
q.s. |
436 |
Paracetamol and CaffeineTablets IP |
Each Film Coated Tablet contains:
Paracetamol
Caffeine
Excipients
Approved Colour used. |
IP
IP |
650mg
50mg
q.s. |
437 |
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. |
438 |
Paracetamol Tablets IP |
Each uncoated tablet contains:-
Paracetamol
Excipients
Colour:-Approved colour used |
IP |
650 mg
q.s. |
439 |
Paracetamol Tablets IP |
Each uncoated tablet contains:-
Paracetamol
Excipients
Approved colour used |
IP |
500 mg
q.s. |
440 |
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 |
441 |
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. |
442 |
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 |
443 |
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 |
444 |
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. |
445 |
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. |
446 |
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. |
447 |
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. |
448 |
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. |
449 |
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. |
450 |
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. |
451 |
Paroxetine Hydrochloride Tablet |
Each film coated Tablet Contains :
Paroxetinehydrochloride Hemihydrate
Equ. to Paroxetine
Excipients
Approved Colour used |
IP |
20mg
q.s |
452 |
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 |
453 |
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 |
454 |
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. |
455 |
Phenytoin Tablets IP |
Each film coated tablet contains:-
Phenytoin Sodium
Excipients
Colour : Approved Coloured Used |
IP |
100 mg
q.s. |
456 |
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. |
457 |
Piracetam Tablets |
Each film coated tablet contains:
Piracetam
Excipients
Approved colour used |
IP |
800 mg
q.s. |
458 |
Piracetam Tablets IP |
Each film coatedtablet contain:
Piracetam
Excipients
Approved colour used |
IP |
400 mg
q.s. |
459 |
Piroxicame DispersibleTablets |
Each uncoated dispersible tablet contains:
Piroxicame
Excipients
Approved colour used |
IP |
20 mg
q.s. |
460 |
Prasugrel Hydrochloride Tablets |
Each Film coated Tablet Contains :
Prasugrel Hydrochloride
Equ. to Prasugrel
Excipients
Approved colour used. |
|
5mg
q.s. |
461 |
Prasugrel Hydrochloride Tablets |
Each Film coated Tablet Contains :
Prasugrel Hydrochloride
Equ. to Prasugrel
Excipients
Approved colour used |
|
10mg
q.s. |
462 |
Prazosin Tablets IP |
Each uncoated tablet contains:
Prazosin Hydrochloride
Eq.to Prazosin
Excipients
Approved colour used. |
IP |
5mg
q.s. |
463 |
Prednisolone Tablet IP |
Each uncoated Tablet contains:
Prednisolone
Excipients
Colour : Approved Coloured Used |
IP |
5mg
q.s |
464 |
Prednisolone Tablet IP |
Each uncoated Tablet contains:
Prednisolone
Excipients
Colour : Approved Coloured Used |
IP |
10mg
q.s |
465 |
Prednisolone Tablet IP |
Each uncoated Tablet contains
Prednisolone
Excipients
Colour : Approved Coloured Used |
IP |
20mg
q.s |
466 |
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. |
467 |
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. |
468 |
Pregabalin Sustained Release Tablet |
Each Uncoated Sustained Release Tablet Contains :
Pregabalin
Excipients
Approved colour used |
IP |
75mg
q.s. |
469 |
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 |
470 |
Pregabalin( Sustained Release) & Methylcobalamin Tablets |
Each film coatedTablet Contains:
Pregabalin
( AsSustained Release)
Methylcobalamin
Excipients
Approved Colour Used. |
IP
IP |
75mg
1500mcg
q.s. |
471 |
Prochlorperazine Maleate Mouth Dissolving Tablets |
Each uncoated Tablet contains:
Prochlorperazine Maleate
Excipients |
IP |
5mg
q.s. |
472 |
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. |
473 |
Propranolol Hydrochloride Tablets |
Each Uncoated Tablet Contains:
Propranolol Hydrochloride
Excipients |
IP |
40mg
q.s. |
474 |
Prulifloxacin Tablets |
Each film coated Tablet Contains:
Prulifloxacin
Excipients
Approved Colour used |
|
600mg |
475 |
Pyridoxine Hydrochloride Tablets IP |
Each uncoated Tablet Contains:
Pyridoxine Hydrochloride
Excipients |
IP |
50mg
q.s. |
476 |
Rabeprazole & Domperidone Tablets |
Each entericcoatedtablets contains:
Rabeprazole Sodium
Domperidone
Excipients
Colour:-Approved colour used |
IP
IP |
20 mg
10 mg
q.s |
477 |
Rabeprazole Gastro- Resistant Tablets IP |
Each entericcoatedtablets contains:
Rabeprazole Sodium
Excipients
Colour:-Approved colour used |
IP |
20mg
q.s |
478 |
Ramipril & Hydrochlorothiazid e Tablets IP |
Each uncoated Tablet Contains:
Ramipril
Hydrochlorthiazide
Excipients
Approved colour used |
IP
IP |
2.5mg
12.5mg
q.s. |
479 |
Ramipril & Hydrochlorothiazid e Tablets IP |
Each uncoated Tablet Contains:
Ramipril
Hydrochlorthiazide
Excipients
Approved colour used |
IP
IP |
5mg
12.5mg
q.s. |
480 |
Ramipril Tablets IP |
Each Uncoated Tablet Contains:
Ramipril
Excipients |
IP |
2.5mg
q.s. |
481 |
Ramipril Tablets IP |
Each uncoated Tablet Contains:
Ramipril
Excipients
Approved colour used |
IP |
1.25 mg
q.s. |
482 |
Ramipril Tablets IP |
Each uncoated Tablet Contains:
Ramipril
Excipients
Approved colour used |
IP |
5mg
q.s. |
483 |
Ranitidine Hydrochloride Tablets |
Each film coated Tablet contains:
Ranitidine Hydrochloride
Equ. to Ranitidine
Excipients
Approved colour used |
IP |
150mg
q. |
484 |
Ranitidine Hydrochloride Tablets |
Each film coated Tablet contains:
Ranitidine Hydrochloride
Equ. to Ranitidine
Excipients
Approved colour used. |
IP |
300mg
q.s |
485 |
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 |
486 |
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. |
487 |
Rifaximin Tablets |
Each filmcoatedtablets contains:
Rifaximin
Excipients
Approved colour used |
|
550 mg
q.s. |
488 |
Rifaximin Tablets |
Each filmcoated tablets contains:
Rifaximin
Excipients
Approved colour used |
|
400 mg
q.s. |
489 |
RifaximineTablets |
Each filmcoated tablets contains:
Rifaximine
Excipients
Approved colour used |
|
200 mg
q.s. |
490 |
Rosuvastatin & FenofibrateTablets |
Each film coated Tablet Contains:
Rosuvastatin Calcium
Equ. to Rosuvastatin
Fenofibrate
Excipients
Approved colour used |
IP
IP |
20mg
160mg
q.s. |
491 |
Rosuvastatin & FinofibrateTablet IP |
Each film coated tablet contains:-
Rosuvastatin calcium
Equ. toRosuvastatin
Finofibrate
Excipients
Colour : Approved Coloured Used |
IP
IP |
10mg
160mg
q.s. |
492 |
Rosuvastatin Tablet IP |
Each film coated tablet Contains :
Rosuvastatin Calcium
Equ. to Rosuvastatin
Excipients
Approved Colour Used |
IP |
40mg |
493 |
Rosuvastatin Tablets IP |
Each filmcoated tablet contain
Rosuvastatin Calcium
Eq.to Rosuvastatin
Excipients
Approved colour used |
IP |
5 mg
q.s. |
494 |
Rosuvastatin Tablets IP |
Each filmcoated tablet contain
Rosuvastatin calcium
Eq.to Rosuvastatin
Excipients
Approved colour used |
IP |
10 mg
q.s. |
495 |
Rosuvastatin Tablets IP |
Each filmcoated tablet contain
Rosuvastatin Calcium
Eq.to Rosuvastatin
Excipients
Approved colour used |
IP |
20 mg
q.s. |
496 |
Roxithromycin & Ambroxol Tablets |
Each film coatedtablet contain:
Roxithromycin
Ambroxol Hydrochloride
Excipients
Approved colour used |
IP
IP |
150 mg
60 mg
q.s |
497 |
Roxithromycin Tablets |
Each filmcoated tablets contains:
Roxithromycin
Excipients
Approved colour used |
IP |
150 mg
q.s. |
498 |
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 |
499 |
Sertraline Hydrochloride Tablets IP |
Each film coated Tablet Contains:
Sertraline Hydrochloride
Equ. To
Sertraline
Excipients
ApprovedColour used. |
IP |
50mg
q.s. |
500 |
Sertraline Tablets IP |
Each film coated tablets contains:
Sertraline Hydrochloride
Eq. to Sertraline
Excipients
Approved colour used. |
IP |
25mg
q.s. |
501 |
Sevelamer Carbonate Tablets |
Each film coated Tablet Contains:
Sevelamer Carbonate
Excipients
Approved colour used |
|
400mg
q.s. |
502 |
Sildenafil Citrate Tablets IP |
Each film coated tablet contains:-
Sildenafil Citrate
Eq. tosildenafil
Excipients
Colour:- Approved Colour used |
IP |
50 mg
q.s |
503 |
Sildenafil Citrate Tablets IP |
Each film coated tablet contains:-
Sildenafil Citrate
Eq. tosildenafil
Excipients
Colour:- Approved Colour used |
IP |
100 mg
q.s. |
504 |
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. |
505 |
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. |
506 |
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. |
507 |
Sitagliptin PhosphateTablet |
Each film coated Tablet Contains :
Sitagliptin phosphate Monohydrate
Equ. to Sitagliptin
Excipients
Approved Colour used |
IP |
25mg
q.s |
508 |
Sitagliptin PhosphateTablet |
Each film coated Tablet Contains :
Sitagliptin phosphate Monohydrate
Equ. to Sitagliptin
Excipients
Approved Colour used |
IP |
50mg
q.s |
509 |
Sitagliptin PhosphateTablet |
Each film coated Tablet Contains :
Sitagliptin phosphate Monohydrate
Equ. to Sitagliptin
Excipients
Approved Colour used |
IP |
100mg
q.s |
510 |
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. |
511 |
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. |
512 |
Solifenacin Succinate Tablets IP |
Each film coated tablet contains:
Solifenacin Succinate
Excipients
Approved colour used. |
IP |
5mg
q.s. |
513 |
Spironolactone Tablets IP |
Each Uncoated Tablet Contains:
Spironolactone
Excipients
Approved colour used |
IP |
25mg
q.s. |
514 |
Spironolactone Tablets IP |
Each Uncoated Tablet Contains:
Spironolactone
Excipients
Approved colour used |
IP |
50mg
q.s. |
515 |
Spironolactone Tablets IP |
Each Uncoated Tablet Contains:
Spironolactone
Excipients
Approved colour used |
IP |
100mg
q.s. |
516 |
Sulfasalazine Gastro –Resistant Tablets IP |
Each enteric coated tablet contains:
Sulfasalazine
Excipients
Approved colour used. |
IP |
500mg
q.s. |
517 |
Sulfasalazine Gastro Resistant Tablets USP |
Each Enteric Coated Tablet Contains:
Sulfasalazine
Excipients
Approved colour used |
USP |
1000mg
q.s. |
518 |
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. |
519 |
Tadalafil Tablet IP |
Each uncoated tablet contains:
Tadalafil
Excipients
Approved colour used |
IP |
10 mg
q.s |
520 |
Tadalafil Tablet IP |
Each uncoated tablet contains:
Tadalafil
Excipients
Approved colour used |
IP |
20 mg
q.s |
521 |
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. |
522 |
Tamsulosin Hydrochloride Modified Release Tablets |
Each film coated Tablet contains:
Tamsulosin Hydrochloride
(as modified release)
Excipients
Approved colour used. |
IP |
0.4mg
q.s. |
523 |
Tapentadol Tablets |
Each film coatedtablet contain:
Tapentadol Hydrochloride
Equivalent to Tapentadol
Excipients
Approved colour used |
IP |
50 mg
q.s. |
524 |
Tapentadol Tablets |
Each film coatedtablet contain:
Tapentadol Hydrochloride
Equivalent to Tapentadol
Excipients
Approved colour used |
IP |
100 mg
q.s. |
525 |
Telmisartan & AmlodipineTablets |
Each uncoated Bilayered Tablet Contains:
Telmisartan
Amlodipine Besylate
Equ. To
Amlodipine
Excipients
Approved colour used |
IP
IP |
80mg
5mg
q.s. |
526 |
Telmisartan & AmlodipineTablets IP |
Each Uncoated Tablet Contains :-
Telmisartan
Amlodipine Besylate
Equ. To Amlodipine
Excipients
Colour: Approved Colour Used. |
IP
IP |
40mg
5mg
q.s. |
527 |
Telmisartan & AmlodipineTablets IP |
Each Uncoated Tablet Contains:-
Telmisartan
Amlodipine Besylate
Equ. To Amlodipine
Excipients
Colour: Approved Coloured Used |
IP
IP |
80mg
10mg
q.s |
528 |
Telmisartan & AmlodipineTablets IP |
Each Uncoated Tablet Contains :-
Telmisartan
Amlodipine Besylate
Equ. To Amlodipine
Excipients
Approved Colour Used. |
IP
IP |
80mg
5mg
q.s. |
529 |
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. |
530 |
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 |
531 |
Telmisartan & Atorvastatin Tablets |
Each film coated Tablet Contains :
Telmisartan
Atorvastatin Calcium
Equ. to Atorvastatin.
Excipients
Approved colour used. |
IP
IP |
40mg
10mg
q.s. |
532 |
Telmisartan & Chlorthalidone Tablets |
Each uncoated Bilayered Tablet contains:
Telmisartan
Chlorthalidone
Excipients
Approved colour used |
IP
IP |
40mg
12.5mg
q.s. |
533 |
Telmisartan & CilnidipineTablets |
Each Film coated Tablet Contains :
Telmisartan
Cilnidipine
Excipients
Approved colour used. |
IP
IP |
40mg
10mg
q.s. |
534 |
Telmisartan & Hydrochlorthiazide Tablet IP |
Each Uncoated Tablet Contains:-
Telmisartan
Hydrochlorothiazide
Excipients
Colour: Approved Coloured Used. |
IP
IP |
80mg
12.5mg
q.s |
535 |
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. |
536 |
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. |
537 |
Telmisartan and Hydrochlorothiazid e TabletsIP |
Each Uncoated Tablet Contains:-
Telmisartan
Hydrochlorothiazide
Excipients
Colour: ApprovedColour Used. |
IP
IP |
40mg
12.5mg
q.s. |
538 |
Telmisartan Tablet IP |
Each Uncoated Tablet Contains:-
Telmisartan
Excipients
Colour: Approved Colour Used. |
IP |
20mg
q.s |
539 |
Telmisartan Tablet IP |
Each Uncoated Tablet Contains:-
Telmisartan
Excipients
Colour: Approved Colour Used. |
IP |
40mg
q.s |
540 |
Telmisartan Tablet IP |
Each Uncoated Tablet Contains:-
Telmisartan
Excipients
Colour: Approved Colour Used. |
IP |
80mg
q.s |
541 |
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 |
542 |
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. |
543 |
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. |
544 |
Terbinafine hydrochloride Tablets IP |
Each filmcoated tablets contains:
Terbinafine hydrochloride
Equivalent to Terbinafine
Excipients
Approved colour used |
IP |
250 mg
q.s. |
545 |
Terbinafine hydrochloride Tablets IP |
Each film coated tablets contains:
Terbinafine hydrochloride
Equivalent to Terbinafine
Excipients
Approved colour used |
IP |
500 mg
q.s. |
546 |
Thiamine Hydrochloride Tablets IP |
Each film coated Tablet Contains:
Thiamine Hydrochloride
Excipients
Approved colour used |
IP |
100mg
q.s. |
547 |
Thiamine Tablets IP |
Each uncoated Tablet Contains
Thiamine Hydrochloride
Excipients
Colour :- Approved colour used |
IP |
50mg
q.s |
548 |
Thyroxine Tablet IP |
Each Uncoated Tablet Contains
Thyroxine sodium
(as anhydrous)
Excipients
Colour : Approved Coloured Used |
IP |
12.5mcg
q.s |
549 |
Thyroxine Tablet IP |
Each Uncoated Tablet Contains
Thyroxine sodium
(as anhydrous)
Excipients
Colour : Approved Coloured Used |
IP |
25mcg
q.s |
550 |
Thyroxine Tablet IP |
Each Uncoated Tablet Contains
Thyroxine sodium
(as anhydrous)
Excipients
Colour : Approved Coloured Used |
IP |
50mcg
q.s |
551 |
Thyroxine Tablet IP |
Each Uncoated Tablet Contains
Thyroxine sodium
(as anhydrous)
Excipients
Colour : Approved Coloured Used |
IP |
75mcg
q.s |
552 |
Thyroxine Tablet IP |
Each Uncoated Tablet Contains
Thyroxine sodium
(as anhydrous)
Excipients
Colour : Approved Coloured Used |
IP |
100 mcg
q.s |
553 |
Ticagrelor Tablets |
Each film coated tablet contains:
Ticagrelor
Excipients
Approved colour used |
IP |
90mg
q.s |
554 |
Tolperisone Hydrochloride & Diclofenac Sodium Tablets |
Each Film coated Tablets Contains :
Tolperisone Hydrochloride
Diclofenac Sodium
Excipients
Approved colour used |
IP
IP |
150mg
50mg
q.s. |
555 |
Tolperisone Hydrochloride & Paracetamol Tablet |
Each film coated Tablet Contains:
Tolperisone hydrochloride
Paracetamol
Excipients
Approved colour Used |
JP
IP |
150mg
325mg |
556 |
Tolperisone Hydrochloride Sustained Release Tablet |
Each film coated sustained Release Tablet Contains:
Tolperisone Hydrochloride
Excipients
Approved Colour Used |
JP |
450mg |
557 |
Tolperisone Hydrochloride Tablet |
Each film coated Tablet Contains:
Tolperisone Hydrochloride
Excipients
Approved colour used |
JP |
150mg
q.s |
558 |
Torsemide & Spironolactone Tablets |
Each uncoated tablet contain:
Torsemide
Spironolactone
Excipients
Approved colour used |
IP
IP |
10 mg
50 mg
q.s. |
559 |
Torsemide & Spironolactone Tablets |
Each uncoated tablet contain:
Torsemide
Spironolactone
Excipients
Approved colour used |
IP
IP |
20 mg
50 mg
q.s. |
560 |
Torsemide & Spironolactone Tablets |
Each uncoated tablet contains:
Torsemide
Spironolactone
Excipients
Approved colour used |
IP
IP |
5 mg
50 mg
q.s. |
561 |
Torsemide Tablets IP |
Each uncoated tablet contain:
Torsemide
Excipients
Approved colour used |
IP |
10 mg
q.s. |
562 |
Torsemide Tablets IP |
Each uncoated tablet contain:
Torsemide
Excipients
Approved colour used |
IP |
20 mg
q.s. |
563 |
Torsemide Tablets IP |
Each uncoated tablet contain:
Torsemide
Excipients
Approved colour used |
IP |
5 mg
q.s. |
564 |
Torsemide Tablets IP |
Each uncoated tablet contain:
Torsemide
Excipients
Approved colour used |
IP |
100 mg
q.s. |
565 |
Tramadol & ParacetamolTablet |
Each Film Coated Tablet Contains:
Paracetamol
Tramadol Hydrochloride
Excipients
Approved Colour Used |
IP
IP |
325mg
37.5mg
q.s |
566 |
Tramadol Hydrochloride Prolonged Release Tablet IP |
Each film coated sustainedrelease tablet contain:
Tramadol Hydrochloride
Excipients
Approved colour used |
IP |
100mg
q.s |
567 |
Tramadol Hydrochloride Tablet IP |
Each film coatedtablet contain:
Tramadol Hydrochloride
Excipients
Approved colour used |
IP |
100mg
q.s |
568 |
Tranexamic Acid & Ethamsylate Tablets |
Each film coated Tablet contains:
Tranexamic Acid
Ethamsylate
Excipients
Approved colour used. |
IP
BP |
250mg
250mg
q.s. |
569 |
Tranexamic Acid Tablets |
Each film coated Tablet Contains:
Tranexamic Acid
Excipients
Colour : Approved Coloured Used |
BP |
250mg
q.s |
570 |
Tranexamic Acid Tablets IP |
Each film coated Tablet Contains:
Tranexamic Acid
Excipients
Approved Colour Used. |
IP |
500mg |
571 |
Tranexamic Acid Tablets IP |
Each film coated Tablet Contains:
Tranexamic Acid
Excipients
Colour : Approved Coloured Used |
IP |
250mg
q.s |
572 |
TranexamicAcid& Mefenamic Acid Tablets |
Each filmcoated tablets contains:
Tranexamic Acid
Mefenamic Acid
Excipients
Approved colour used |
IP
IP |
500 mg
250 mg
q.s. |
573 |
Trifluoperazine Hydrochloride Tablets IP |
Each film coated Tablet contains:
Trifluoperazine Hydrochloride
Excipients
Approved colour used |
IP |
5mg
q.s |
574 |
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. |
575 |
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. |
576 |
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. |
|
577 |
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. |
578 |
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. |
579 |
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. |
580 |
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 |
581 |
Ursodeoxycholic Acid Tablets IP |
Each filmcoated tablets contains:
Ursodeoxycholic Acid
Excipients
Approved colour used |
IP |
300 mg
q.s. |
582 |
Ursodeoxycholic Acid Tablets IP |
Each film coated tablets contains:
Ursodeoxycholic Acid
Excipients
Approved colour used |
IP |
150 mg
q.s. |
583 |
Vildagliptin & Metformin Hydrochloride Tablet |
Each film coated tablet contains:
Vildagliptin
Metformin Hydrochloride
Excipients
Approved colour used |
IP |
50 mg
500 mg
q.s. |
584 |
Vildagliptin & Metformin Hydrochloride Tablet |
Each film coated tablet contains:
Vildagliptin
Metformin Hydrochloride
Excipients
Approved colour used |
IP |
50 mg
1000 mg
q.s. |
585 |
Vildagliptin Tablet |
Each uncoatedtablet contains:
Vildagliptin
Excipients
Approved colour used |
|
50 mg
q.s. |
586 |
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 |
587 |
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. |
588 |
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. |
589 |
Voglibose Dispersible Tablet IP |
Each uncoated tablet contains:
Voglibose
Excipients
Approved colour used |
IP |
0.2 mg
q.s. |
590 |
Voglibose Dispersible Tablet IP |
Each uncoated tablet contains:
Voglibose
Excipients
Approved colour used |
IP |
0.3 mg
q.s. |
591 |
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. |
592 |
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. |
593 |
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. |
594 |
Voriconazole Tablet IP |
Each film coated Tablet Contains:
Voriconazole
Excipients
Approved Colour Used. |
IP |
200 mg
q.s |
595 |
Warfarin Sodium Tablets IP 1mg |
Each uncoated tablet contains:
Warfarin Sodium Clathrate
Eq. to Warfarin Sodium
(anhydrous)
Excipients
ApprovedColour used |
IP |
1mg
q.s. |
596 |
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. |
597 |
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. |
598 |
Zinc Acetate Tablets |
Each Enteric coated Tablet Contains:
Zinc Acetate(as dihydrate)
Equ. toElemental Zinc
Excipients
Approved Colour Used |
USP |
50mg
q.s |