FdaApplication
ANDA 074936
Identifiers
- fda_app_no: ANDA074936
Properties
| Property | Value |
|---|---|
| applicant_name | ACTAVIS ELIZABETH LLC |
| application_type | ANDA |
| approval_date | 1998-02-24 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| NAPROXEN | NAPROXEN | 375MG | TABLET, DELAYED RELEASE;ORAL |
| NAPROXEN | NAPROXEN | 500MG | TABLET, DELAYED RELEASE;ORAL |
2 products