FdaApplication
ANDA 088867
Identifiers
- fda_app_no: ANDA088867
Properties
| Property | Value |
|---|---|
| applicant_name | SUPERPHARM CORP |
| application_type | ANDA |
| approval_date | 1984-10-25 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PREDNISONE | PREDNISONE | 20MG | TABLET;ORAL |
1 product