FdaApplication
ANDA 079096
Identifiers
- fda_app_no: ANDA079096
Properties
| Property | Value |
|---|---|
| applicant_name | AMNEAL PHARMACEUTICALS NY LLC |
| application_type | ANDA |
| approval_date | 2008-12-16 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| NAPROXEN SODIUM | NAPROXEN SODIUM | 220MG | TABLET;ORAL |
1 product