FdaApplication
ANDA 075168
Identifiers
- fda_app_no: ANDA075168
Properties
| Property | Value |
|---|---|
| applicant_name | DR REDDYS LABORATORIES INC |
| application_type | ANDA |
| approval_date | 1998-07-28 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| NAPROXEN SODIUM | NAPROXEN SODIUM | 220MG | TABLET;ORAL |
1 product