FdaApplication
ANDA 088892
Identifiers
- fda_app_no: ANDA088892
Properties
| Property | Value |
|---|---|
| applicant_name | SUPERPHARM CORP |
| application_type | ANDA |
| approval_date | 1985-02-26 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PREDNISOLONE | PREDNISOLONE | 5MG | TABLET;ORAL |
1 product