FdaApplication
ANDA 215106
Identifiers
- fda_app_no: ANDA215106
Properties
| Property | Value |
|---|---|
| applicant_name | AMNEAL EU LTD |
| application_type | ANDA |
| approval_date | 2021-10-14 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| DEXAMETHASONE | DEXAMETHASONE | 4MG | TABLET;ORAL |
| DEXAMETHASONE | DEXAMETHASONE | 6MG | TABLET;ORAL |
2 products