FdaApplication
ANDA 072981
Identifiers
- fda_app_no: ANDA072981
Properties
| Property | Value |
|---|---|
| applicant_name | WATSON LABORATORIES INC |
| application_type | ANDA |
| approval_date | 1991-08-19 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| FENOPROFEN CALCIUM | FENOPROFEN CALCIUM | EQ 200MG BASE | CAPSULE;ORAL |
1 product