FdaApplication
ANDA 074285
Identifiers
- fda_app_no: ANDA074285
Properties
| Property | Value |
|---|---|
| applicant_name | PUREPAC PHARMACEUTICAL CO |
| application_type | ANDA |
| approval_date | 1996-05-07 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| DIFLUNISAL | DIFLUNISAL | 250MG | TABLET;ORAL |
| DIFLUNISAL | DIFLUNISAL | 500MG | TABLET;ORAL |
2 products