FdaApplication
ANDA 072437
Identifiers
- fda_app_no: ANDA072437
Properties
| Property | Value |
|---|---|
| applicant_name | PAR PHARMACEUTICAL INC |
| application_type | ANDA |
| approval_date | 1988-08-22 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| FENOPROFEN CALCIUM | FENOPROFEN CALCIUM | EQ 200MG BASE | CAPSULE;ORAL |
1 product