FdaApplication
ANDA 070709
Identifiers
- fda_app_no: ANDA070709
Properties
| Property | Value |
|---|---|
| applicant_name | SUPERPHARM CORP |
| application_type | ANDA |
| approval_date | 1986-04-25 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| IBUPROFEN | IBUPROFEN | 600MG | TABLET;ORAL |
1 product