FdaApplication
ANDA 070437
Identifiers
- fda_app_no: ANDA070437
Properties
| Property | Value |
|---|---|
| applicant_name | WATSON LABORATORIES INC |
| application_type | ANDA |
| approval_date | 1985-08-21 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| IBUPROFEN | IBUPROFEN | 600MG | TABLET;ORAL |
1 product