| 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) |
| 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) |
| 70710-1832-0 |
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) |
| 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) |
| 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) |
| 60290-057-02 |
60290-057 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Potassium |
Diclofenac Potassium Tablets |
TABLET, FILM COATED |
ORAL |
20220512 |
N/A |
ANDA |
ANDA215750 |
Umedica Laboratories USA Inc. |
DICLOFENAC POTASSIUM |
50 mg/1 |
1000 TABLET, FILM COATED in 1 BOTTLE (60290-057-02) |
| 60290-057-03 |
60290-057 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Potassium |
Diclofenac Potassium Tablets |
TABLET, FILM COATED |
ORAL |
20220512 |
N/A |
ANDA |
ANDA215750 |
Umedica Laboratories USA Inc. |
DICLOFENAC POTASSIUM |
50 mg/1 |
500 TABLET, FILM COATED in 1 BOTTLE (60290-057-03) |
| 60290-057-01 |
60290-057 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Potassium |
Diclofenac Potassium Tablets |
TABLET, FILM COATED |
ORAL |
20220512 |
N/A |
ANDA |
ANDA215750 |
Umedica Laboratories USA Inc. |
DICLOFENAC POTASSIUM |
50 mg/1 |
100 TABLET, FILM COATED in 1 BOTTLE (60290-057-01) |
| 60290-088-02 |
60290-088 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Potassium |
Diclofenac Potassium Tablets |
TABLET, FILM COATED |
ORAL |
20240928 |
N/A |
ANDA |
ANDA215750 |
Umedica Laboratories USA Inc. |
DICLOFENAC POTASSIUM |
25 mg/1 |
100 TABLET, FILM COATED in 1 BOTTLE (60290-088-02) |
| 60290-088-05 |
60290-088 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Potassium |
Diclofenac Potassium Tablets |
TABLET, FILM COATED |
ORAL |
20251030 |
N/A |
ANDA |
ANDA215750 |
Umedica Laboratories USA Inc. |
DICLOFENAC POTASSIUM |
25 mg/1 |
60 TABLET, FILM COATED in 1 BOTTLE (60290-088-05) |
| 60290-088-03 |
60290-088 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Potassium |
Diclofenac Potassium Tablets |
TABLET, FILM COATED |
ORAL |
20240928 |
N/A |
ANDA |
ANDA215750 |
Umedica Laboratories USA Inc. |
DICLOFENAC POTASSIUM |
25 mg/1 |
500 TABLET, FILM COATED in 1 BOTTLE (60290-088-03) |
| 60290-088-01 |
60290-088 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Potassium |
Diclofenac Potassium Tablets |
TABLET, FILM COATED |
ORAL |
20240928 |
N/A |
ANDA |
ANDA215750 |
Umedica Laboratories USA Inc. |
DICLOFENAC POTASSIUM |
25 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE (60290-088-01) |
| 60290-088-04 |
60290-088 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Potassium |
Diclofenac Potassium Tablets |
TABLET, FILM COATED |
ORAL |
20240928 |
N/A |
ANDA |
ANDA215750 |
Umedica Laboratories USA Inc. |
DICLOFENAC POTASSIUM |
25 mg/1 |
1000 TABLET, FILM COATED in 1 BOTTLE (60290-088-04) |
| 71335-9720-1 |
71335-9720 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Potassium |
Diclofenac Potassium Tablets |
TABLET, FILM COATED |
ORAL |
20250203 |
N/A |
ANDA |
ANDA215750 |
Bryant Ranch Prepack |
DICLOFENAC POTASSIUM |
50 mg/1 |
20 TABLET, FILM COATED in 1 BOTTLE (71335-9720-1) |
| 71335-9720-5 |
71335-9720 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Potassium |
Diclofenac Potassium Tablets |
TABLET, FILM COATED |
ORAL |
20250203 |
N/A |
ANDA |
ANDA215750 |
Bryant Ranch Prepack |
DICLOFENAC POTASSIUM |
50 mg/1 |
45 TABLET, FILM COATED in 1 BOTTLE (71335-9720-5) |
| 71335-9720-6 |
71335-9720 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Potassium |
Diclofenac Potassium Tablets |
TABLET, FILM COATED |
ORAL |
20250203 |
N/A |
ANDA |
ANDA215750 |
Bryant Ranch Prepack |
DICLOFENAC POTASSIUM |
50 mg/1 |
58 TABLET, FILM COATED in 1 BOTTLE (71335-9720-6) |
| 71335-9720-7 |
71335-9720 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Potassium |
Diclofenac Potassium Tablets |
TABLET, FILM COATED |
ORAL |
20250203 |
N/A |
ANDA |
ANDA215750 |
Bryant Ranch Prepack |
DICLOFENAC POTASSIUM |
50 mg/1 |
18 TABLET, FILM COATED in 1 BOTTLE (71335-9720-7) |
| 71335-9720-8 |
71335-9720 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Potassium |
Diclofenac Potassium Tablets |
TABLET, FILM COATED |
ORAL |
20250203 |
N/A |
ANDA |
ANDA215750 |
Bryant Ranch Prepack |
DICLOFENAC POTASSIUM |
50 mg/1 |
120 TABLET, FILM COATED in 1 BOTTLE (71335-9720-8) |
| 71335-9720-2 |
71335-9720 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Potassium |
Diclofenac Potassium Tablets |
TABLET, FILM COATED |
ORAL |
20231017 |
N/A |
ANDA |
ANDA215750 |
Bryant Ranch Prepack |
DICLOFENAC POTASSIUM |
50 mg/1 |
90 TABLET, FILM COATED in 1 BOTTLE (71335-9720-2) |