FdaApplication
ANDA 074263
Identifiers
- fda_app_no: ANDA074263
Properties
| Property | Value |
|---|---|
| applicant_name | PUREPAC PHARMACEUTICAL CO |
| application_type | ANDA |
| approval_date | 1993-12-21 |
Products (3)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| NAPROXEN | NAPROXEN | 250MG | TABLET;ORAL |
| NAPROXEN | NAPROXEN | 375MG | TABLET;ORAL |
| NAPROXEN | NAPROXEN | 500MG | TABLET;ORAL |
3 products