FdaApplication
ANDA 087986
Identifiers
- fda_app_no: ANDA087986
Properties
| Property | Value |
|---|---|
| applicant_name | UDL LABORATORIES INC |
| application_type | ANDA |
| approval_date | 1983-01-18 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PREDNISONE | PREDNISONE | 20MG | TABLET;ORAL |
1 product