FdaApplication
ANDA 071664
Identifiers
- fda_app_no: ANDA071664
Properties
| Property | Value |
|---|---|
| applicant_name | PUREPAC PHARMACEUTICAL CO |
| application_type | ANDA |
| approval_date | 1987-02-03 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| IBUPROFEN | IBUPROFEN | 200MG | TABLET;ORAL |
1 product