29300-381-05 |
29300-381 |
HUMAN PRESCRIPTION DRUG |
divalproex sodium |
divalproex sodium |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20220715 |
N/A |
ANDA |
ANDA214643 |
Unichem Pharmaceuticals (USA), Inc. |
DIVALPROEX SODIUM |
500 mg/1 |
500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (29300-381-05) |
29300-381-01 |
29300-381 |
HUMAN PRESCRIPTION DRUG |
divalproex sodium |
divalproex sodium |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20220715 |
N/A |
ANDA |
ANDA214643 |
Unichem Pharmaceuticals (USA), Inc. |
DIVALPROEX SODIUM |
500 mg/1 |
100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (29300-381-01) |
29300-380-05 |
29300-380 |
HUMAN PRESCRIPTION DRUG |
divalproex sodium |
divalproex sodium |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20220715 |
N/A |
ANDA |
ANDA214643 |
Unichem Pharmaceuticals (USA), Inc. |
DIVALPROEX SODIUM |
250 mg/1 |
500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (29300-380-05) |
29300-380-01 |
29300-380 |
HUMAN PRESCRIPTION DRUG |
divalproex sodium |
divalproex sodium |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20220715 |
N/A |
ANDA |
ANDA214643 |
Unichem Pharmaceuticals (USA), Inc. |
DIVALPROEX SODIUM |
250 mg/1 |
100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (29300-380-01) |