FdaApplication
ANDA 087701
Identifiers
- fda_app_no: ANDA087701
Properties
| Property | Value |
|---|---|
| applicant_name | VANGARD LABORATORIES INC DIV MIDWAY MEDICAL CO |
| application_type | ANDA |
| approval_date | 1982-01-15 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PREDNISONE | PREDNISONE | 20MG | TABLET;ORAL |
1 product