FdaApplication
ANDA 207481
Identifiers
- fda_app_no: ANDA207481
Properties
| Property | Value |
|---|---|
| applicant_name | AMNEAL EU LTD |
| application_type | ANDA |
| approval_date | 2021-09-21 |
Products (4)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| METHYLPREDNISOLONE | METHYLPREDNISOLONE | 16MG | TABLET;ORAL |
| METHYLPREDNISOLONE | METHYLPREDNISOLONE | 4MG | TABLET;ORAL |
| METHYLPREDNISOLONE | METHYLPREDNISOLONE | 32MG | TABLET;ORAL |
| METHYLPREDNISOLONE | METHYLPREDNISOLONE | 8MG | TABLET;ORAL |
4 products