75987-010-72 |
75987-010 |
HUMAN PRESCRIPTION DRUG |
DUEXIS |
Ibuprofen and Famotidine |
TABLET, COATED |
ORAL |
20111205 |
20250831 |
NDA |
NDA022519 |
Horizon Therapeutics USA, Inc. |
FAMOTIDINE; IBUPROFEN |
26.6 mg/1; 800 mg/1 |
9 BLISTER PACK in 1 CARTON (75987-010-72) / 3 TABLET, COATED in 1 BLISTER PACK |
75987-010-03 |
75987-010 |
HUMAN PRESCRIPTION DRUG |
DUEXIS |
Ibuprofen and Famotidine |
TABLET, COATED |
ORAL |
20111205 |
20250831 |
NDA |
NDA022519 |
Horizon Therapeutics USA, Inc. |
FAMOTIDINE; IBUPROFEN |
26.6 mg/1; 800 mg/1 |
90 TABLET, COATED in 1 BOTTLE (75987-010-03) |
70748-312-09 |
70748-312 |
HUMAN PRESCRIPTION DRUG |
Ibuprofen and Famotidine |
Ibuprofen and Famotidine |
TABLET, COATED |
ORAL |
20210914 |
N/A |
NDA AUTHORIZED GENERIC |
NDA022519 |
Lupin Pharmaceuticals, Inc. |
FAMOTIDINE; IBUPROFEN |
26.6 mg/1; 800 mg/1 |
90 TABLET, COATED in 1 BOTTLE (70748-312-09) |