Lupin Ltd Unclassified
FDA Approved Drugs
Lupin Ltd Unclassified
FDA Approved Drugs Database
FDA approved drug product records including application numbers, product numbers, drug names, active ingredients, dosage forms, strengths, approval dates and regulatory status.
- Total Records 46
- Latest Approval Date -
- Data Source FDA
- First Approval Date -
Company Overview
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Lupin Ltd Unclassified
Kalina, Santacruz East, Mumbai 400 098
India
www.lupin.com/ info@lupin.com View on MapFDA Approved Drug Records ( 46 records )
Drug Name
ABACAVIR; DOLUTEGRAVIR; LAMIVUDINE
Product Number
1
Dosage Form
-
Strength
5MG
Approval Date
-
Active Ingredient
ABACAVIR;DOLUTEGRAVIR;LAMIVUDINE
Application Number
218383
Product Number
1
Dosage Form
-
Strength
5MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
ABACAVIR; DOLUTEGRAVIR; LAMIVUDINE
Product Number
2
Dosage Form
-
Strength
30MG
Approval Date
-
Active Ingredient
ABACAVIR;DOLUTEGRAVIR;LAMIVUDINE
Application Number
218383
Product Number
2
Dosage Form
-
Strength
30MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
ABACAVIR; DOLUTEGRAVIR; LAMIVUDINE
Product Number
3
Dosage Form
-
Strength
60MG
Approval Date
-
Active Ingredient
ABACAVIR;DOLUTEGRAVIR;LAMIVUDINE
Application Number
218383
Product Number
3
Dosage Form
-
Strength
60MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
ARMLUPEG
Product Number
1
Dosage Form
-
Strength
6MG/0.6ML
Approval Date
-
Active Ingredient
PEGFILGRASTIM-UNNE
Application Number
761212
Product Number
1
Dosage Form
-
Strength
6MG/0.6ML
Approval Date
-
Regulatory Status
Unclassified
Drug Name
ARMODAFINIL
Product Number
2
Dosage Form
-
Strength
100MG
Approval Date
-
Active Ingredient
ARMODAFINIL
Application Number
200751
Product Number
2
Dosage Form
-
Strength
100MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
BALSALAZIDE DISODIUM
Product Number
1
Dosage Form
-
Strength
1.1GM
Approval Date
-
Active Ingredient
BALSALAZIDE DISODIUM
Application Number
206529
Product Number
1
Dosage Form
-
Strength
1.1GM
Approval Date
-
Regulatory Status
Unclassified
Drug Name
DAPAGLIFLOZIN AND SAXAGLIPTIN MONOHYDRATE
Product Number
1
Dosage Form
-
Strength
5MG
Approval Date
-
Active Ingredient
DAPAGLIFLOZIN, SAXAGLIPTIN MONOHYDRATE
Application Number
211532
Product Number
1
Dosage Form
-
Strength
5MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
DAPAGLIFLOZIN AND SAXAGLIPTIN MONOHYDRATE
Product Number
2
Dosage Form
-
Strength
10MG
Approval Date
-
Active Ingredient
DAPAGLIFLOZIN, SAXAGLIPTIN MONOHYDRATE
Application Number
211532
Product Number
2
Dosage Form
-
Strength
10MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
DARUNAVIR
Product Number
3
Dosage Form
-
Strength
300MG
Approval Date
-
Active Ingredient
DARUNAVIR
Application Number
202073
Product Number
3
Dosage Form
-
Strength
300MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
DARUNAVIR
Product Number
4
Dosage Form
-
Strength
400MG
Approval Date
-
Active Ingredient
DARUNAVIR
Application Number
202073
Product Number
4
Dosage Form
-
Strength
400MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
DARUNAVIR
Product Number
5
Dosage Form
-
Strength
600MG
Approval Date
-
Active Ingredient
DARUNAVIR
Application Number
202073
Product Number
5
Dosage Form
-
Strength
600MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
DARUNAVIR
Product Number
6
Dosage Form
-
Strength
800MG
Approval Date
-
Active Ingredient
DARUNAVIR
Application Number
202073
Product Number
6
Dosage Form
-
Strength
800MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
DICLOFENAC
Product Number
1
Dosage Form
-
Strength
18MG
Approval Date
-
Active Ingredient
DICLOFENAC
Application Number
207393
Product Number
1
Dosage Form
-
Strength
18MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
DICLOFENAC
Product Number
2
Dosage Form
-
Strength
35MG
Approval Date
-
Active Ingredient
DICLOFENAC
Application Number
207393
Product Number
2
Dosage Form
-
Strength
35MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
DOLUTEGRAVIR; EMTRICITABINE; TENOFOVIR ALAFENAMIDE
Product Number
1
Dosage Form
-
Strength
50MG;200MG;25MG
Approval Date
-
Active Ingredient
DOLUTEGRAVIR;EMTRICITABINE;TENOFOVIR ALAFENAMIDE
Application Number
214544
Product Number
1
Dosage Form
-
Strength
50MG;200MG;25MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
DOLUTEGRAVIR; RILPIVIRINE
Product Number
1
Dosage Form
-
Strength
50MG/25MG
Approval Date
-
Active Ingredient
DOLUTEGRAVIR;RILPIVIRINE
Application Number
213120
Product Number
1
Dosage Form
-
Strength
50MG/25MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
DOXYCYCLINE
Product Number
1
Dosage Form
-
Strength
40MG
Approval Date
-
Active Ingredient
DOXYCYCLINE
Application Number
91277
Product Number
1
Dosage Form
-
Strength
40MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
DROSPIRENONE
Product Number
1
Dosage Form
-
Strength
4MG
Approval Date
-
Active Ingredient
DROSPIRENONE
Application Number
216936
Product Number
1
Dosage Form
-
Strength
4MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
EMPAGLIFLOZIN;METFORMIN HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
5MG; 1GM
Approval Date
-
Active Ingredient
EMPAGLIFLOZIN;METFORMIN HYDROCHLORIDE
Application Number
213654
Product Number
1
Dosage Form
-
Strength
5MG; 1GM
Approval Date
-
Regulatory Status
Unclassified
Drug Name
EMPAGLIFLOZIN;METFORMIN HYDROCHLORIDE
Product Number
2
Dosage Form
-
Strength
10MG; 1GM
Approval Date
-
Active Ingredient
EMPAGLIFLOZIN;METFORMIN HYDROCHLORIDE
Application Number
213654
Product Number
2
Dosage Form
-
Strength
10MG; 1GM
Approval Date
-
Regulatory Status
Unclassified
Drug Name
EMPAGLIFLOZIN;METFORMIN HYDROCHLORIDE
Product Number
3
Dosage Form
-
Strength
12.5MG; 1GM
Approval Date
-
Active Ingredient
EMPAGLIFLOZIN;METFORMIN HYDROCHLORIDE
Application Number
213654
Product Number
3
Dosage Form
-
Strength
12.5MG; 1GM
Approval Date
-
Regulatory Status
Unclassified
Drug Name
EMPAGLIFLOZIN;METFORMIN HYDROCHLORIDE
Product Number
4
Dosage Form
-
Strength
25MG; 1GM
Approval Date
-
Active Ingredient
EMPAGLIFLOZIN;METFORMIN HYDROCHLORIDE
Application Number
213654
Product Number
4
Dosage Form
-
Strength
25MG; 1GM
Approval Date
-
Regulatory Status
Unclassified
Drug Name
EMTRICITABINE; TENOFOVIR ALAFENAMIDE
Product Number
1
Dosage Form
-
Strength
200MG;25MG
Approval Date
-
Active Ingredient
EMTRICITABINE;TENOFOVIR ALAFENAMIDE
Application Number
215071
Product Number
1
Dosage Form
-
Strength
200MG;25MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
FOSAMPRENAVIR CALCIUM
Product Number
1
Dosage Form
-
Strength
700MG
Approval Date
-
Active Ingredient
FOSAMPRENAVIR CALCIUM
Application Number
204130
Product Number
1
Dosage Form
-
Strength
700MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
IVACAFTOR
Product Number
1
Dosage Form
-
Strength
150MG
Approval Date
-
Active Ingredient
IVACAFTOR
Application Number
216074
Product Number
1
Dosage Form
-
Strength
150MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
IVACAFTOR
Product Number
2
Dosage Form
-
Strength
25MG
Approval Date
-
Active Ingredient
IVACAFTOR
Application Number
217431
Product Number
2
Dosage Form
-
Strength
25MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
IVACAFTOR
Product Number
3
Dosage Form
-
Strength
50MG
Approval Date
-
Active Ingredient
IVACAFTOR
Application Number
217431
Product Number
3
Dosage Form
-
Strength
50MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
IVACAFTOR
Product Number
4
Dosage Form
-
Strength
75MG
Approval Date
-
Active Ingredient
IVACAFTOR
Application Number
217431
Product Number
4
Dosage Form
-
Strength
75MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
LEVONORGESTREL
Product Number
2
Dosage Form
-
Strength
0.75MG
Approval Date
-
Active Ingredient
LEVONORGESTREL
Application Number
91328
Product Number
2
Dosage Form
-
Strength
0.75MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
LO-BLISOVI FE
Product Number
1
Dosage Form
-
Strength
1MG;0.01MG;75MG
Approval Date
-
Active Ingredient
NORETHINDRONE ACETATE;ETHINYL ESTRADIOL;FERROUS FUMARATE
Application Number
203113
Product Number
1
Dosage Form
-
Strength
1MG;0.01MG;75MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
MILNACIPRAN HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
12.5MG
Approval Date
-
Active Ingredient
MILNACIPRAN HYDROCHLORIDE
Application Number
205286
Product Number
1
Dosage Form
-
Strength
12.5MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
MILNACIPRAN HYDROCHLORIDE
Product Number
2
Dosage Form
-
Strength
25MG
Approval Date
-
Active Ingredient
MILNACIPRAN HYDROCHLORIDE
Application Number
205286
Product Number
2
Dosage Form
-
Strength
25MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
MILNACIPRAN HYDROCHLORIDE
Product Number
3
Dosage Form
-
Strength
50MG
Approval Date
-
Active Ingredient
MILNACIPRAN HYDROCHLORIDE
Application Number
205286
Product Number
3
Dosage Form
-
Strength
50MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
MILNACIPRAN HYDROCHLORIDE
Product Number
4
Dosage Form
-
Strength
100MG
Approval Date
-
Active Ingredient
MILNACIPRAN HYDROCHLORIDE
Application Number
205286
Product Number
4
Dosage Form
-
Strength
100MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
OXCARBAZEPINE EXTENDED RELEASE TABLETS
Product Number
2
Dosage Form
-
Strength
300MG
Approval Date
-
Active Ingredient
OXCARBAZEPINE
Application Number
219404
Product Number
2
Dosage Form
-
Strength
300MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
OXCARBAZEPINE EXTENDED RELEASE TABLETS
Product Number
3
Dosage Form
-
Strength
600MG
Approval Date
-
Active Ingredient
OXCARBAZEPINE
Application Number
219404
Product Number
3
Dosage Form
-
Strength
600MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
PITOLISANT HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
EQ 4.45MG BASE
Approval Date
-
Active Ingredient
PITOLISANT HYDROCHLORIDE
Application Number
218846
Product Number
1
Dosage Form
-
Strength
EQ 4.45MG BASE
Approval Date
-
Regulatory Status
Unclassified
Drug Name
PITOLISANT HYDROCHLORIDE
Product Number
2
Dosage Form
-
Strength
EQ 17.8MG BASE
Approval Date
-
Active Ingredient
PITOLISANT HYDROCHLORIDE
Application Number
218846
Product Number
2
Dosage Form
-
Strength
EQ 17.8MG BASE
Approval Date
-
Regulatory Status
Unclassified
Drug Name
PREGABALIN
Product Number
1
Dosage Form
-
Strength
20MG/ML
Approval Date
-
Active Ingredient
PREGABALIN
Application Number
201989
Product Number
1
Dosage Form
-
Strength
20MG/ML
Approval Date
-
Regulatory Status
Unclassified
Drug Name
RANLUSPEC
Product Number
1
Dosage Form
-
Strength
10MG/ML
Approval Date
-
Active Ingredient
RANIBIZUMAB-HKDZ
Application Number
761480
Product Number
1
Dosage Form
-
Strength
10MG/ML
Approval Date
-
Regulatory Status
Unclassified
Drug Name
RANLUSPEC
Product Number
2
Dosage Form
-
Strength
6MG/ML
Approval Date
-
Active Ingredient
RANIBIZUMAB-HKDZ
Application Number
761480
Product Number
2
Dosage Form
-
Strength
6MG/ML
Approval Date
-
Regulatory Status
Unclassified
Drug Name
TENOFOVIR DISOPROXIL FUMARATE
Product Number
1
Dosage Form
-
Strength
150MG
Approval Date
-
Active Ingredient
TENOFOVIR DISOPROXIL FUMARATE
Application Number
204402
Product Number
1
Dosage Form
-
Strength
150MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
TENOFOVIR DISOPROXIL FUMARATE
Product Number
2
Dosage Form
-
Strength
200MG
Approval Date
-
Active Ingredient
TENOFOVIR DISOPROXIL FUMARATE
Application Number
204402
Product Number
2
Dosage Form
-
Strength
200MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
TENOFOVIR DISOPROXIL FUMARATE
Product Number
3
Dosage Form
-
Strength
250MG
Approval Date
-
Active Ingredient
TENOFOVIR DISOPROXIL FUMARATE
Application Number
204402
Product Number
3
Dosage Form
-
Strength
250MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
TENOFOVIR DISOPROXIL FUMARATE
Product Number
4
Dosage Form
-
Strength
300MG
Approval Date
-
Active Ingredient
TENOFOVIR DISOPROXIL FUMARATE
Application Number
204402
Product Number
4
Dosage Form
-
Strength
300MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
VALBENAZINE TOSYLATE
Product Number
3
Dosage Form
-
Strength
EQ 60MG BASE
Approval Date
-
Active Ingredient
VALBENAZINE TOSYLATE
Application Number
216064
Product Number
3
Dosage Form
-
Strength
EQ 60MG BASE
Approval Date
-
Regulatory Status
Unclassified
Drug Status Breakdown
46 total- Unclassified
Official Source
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Drug Name
ABACAVIR; DOLUTEGRAVIR; LAMIVUDINE
Application Number
218383
Product Number
1
Active Ingredient
ABACAVIR;DOLUTEGRAVIR;LAMIVUDINE
Dosage Form
-
Strength
5MG
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