FdaApplication
ANDA 213385
Identifiers
- fda_app_no: ANDA213385
Properties
| Property | Value |
|---|---|
| applicant_name | AMNEAL EU LTD |
| application_type | ANDA |
| approval_date | 2020-06-16 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PREDNISONE | PREDNISONE | 1MG | TABLET;ORAL |
| PREDNISONE | PREDNISONE | 5MG | TABLET;ORAL |
2 products