FdaApplication
ANDA 078432
Identifiers
- fda_app_no: ANDA078432
Properties
| Property | Value |
|---|---|
| applicant_name | AMNEAL PHARMACEUTICALS NY LLC |
| application_type | ANDA |
| approval_date | 2007-04-25 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| NAPROXEN SODIUM | NAPROXEN SODIUM | EQ 500MG BASE | TABLET;ORAL |
| NAPROXEN SODIUM | NAPROXEN SODIUM | EQ 250MG BASE | TABLET;ORAL |
2 products