FdaApplication
ANDA 071964
Identifiers
- fda_app_no: ANDA071964
Properties
| Property | Value |
|---|---|
| applicant_name | PUREPAC PHARMACEUTICAL CO |
| application_type | ANDA |
| approval_date | 1988-02-01 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| IBUPROFEN | IBUPROFEN | 800MG | TABLET;ORAL |
1 product