| 70710-1832-0 |
70710-1832 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Potassium |
Diclofenac Potassium Tablets |
TABLET, FILM COATED |
ORAL |
20220512 |
N/A |
ANDA |
ANDA215750 |
Zydus Pharmaceuticals (USA) Inc. |
DICLOFENAC POTASSIUM |
50 mg/1 |
1000 TABLET, FILM COATED in 1 BOTTLE (70710-1832-0) |
| 70710-1832-1 |
70710-1832 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Potassium |
Diclofenac Potassium Tablets |
TABLET, FILM COATED |
ORAL |
20220512 |
N/A |
ANDA |
ANDA215750 |
Zydus Pharmaceuticals (USA) Inc. |
DICLOFENAC POTASSIUM |
50 mg/1 |
100 TABLET, FILM COATED in 1 BOTTLE (70710-1832-1) |
| 70710-1832-5 |
70710-1832 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Potassium |
Diclofenac Potassium Tablets |
TABLET, FILM COATED |
ORAL |
20220512 |
N/A |
ANDA |
ANDA215750 |
Zydus Pharmaceuticals (USA) Inc. |
DICLOFENAC POTASSIUM |
50 mg/1 |
500 TABLET, FILM COATED in 1 BOTTLE (70710-1832-5) |
| 75834-337-30 |
75834-337 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Potassium |
Diclofenac Potassium Tablets |
TABLET, FILM COATED |
ORAL |
20251010 |
N/A |
ANDA |
ANDA215750 |
NIVAGEN PHARMACEUTICALS, INC. |
DICLOFENAC POTASSIUM |
25 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE (75834-337-30) |
| 75834-337-60 |
75834-337 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Potassium |
Diclofenac Potassium Tablets |
TABLET, FILM COATED |
ORAL |
20251010 |
N/A |
ANDA |
ANDA215750 |
NIVAGEN PHARMACEUTICALS, INC. |
DICLOFENAC POTASSIUM |
25 mg/1 |
60 TABLET, FILM COATED in 1 BOTTLE (75834-337-60) |
| 68071-3451-3 |
68071-3451 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Potassium |
Diclofenac Potassium Tablets |
TABLET, FILM COATED |
ORAL |
20230705 |
N/A |
ANDA |
ANDA215750 |
NuCare Pharmaceuticals,Inc. |
DICLOFENAC POTASSIUM |
50 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE (68071-3451-3) |