FdaApplication
ANDA 076494
Identifiers
- fda_app_no: ANDA076494
Properties
| Property | Value |
|---|---|
| applicant_name | HIKMA INTERNATIONAL PHARMACEUTICALS LLC |
| application_type | ANDA |
| approval_date | 2004-01-14 |
Products (3)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| NAPROXEN | NAPROXEN | 500MG | TABLET;ORAL |
| NAPROXEN | NAPROXEN | 250MG | TABLET;ORAL |
| NAPROXEN | NAPROXEN | 375MG | TABLET;ORAL |
3 products