FdaApplication
ANDA 072293
Identifiers
- fda_app_no: ANDA072293
Properties
| Property | Value |
|---|---|
| applicant_name | WATSON LABORATORIES INC |
| application_type | ANDA |
| approval_date | 1988-08-17 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| FENOPROFEN CALCIUM | FENOPROFEN CALCIUM | EQ 300MG BASE | CAPSULE;ORAL |
1 product