FdaApplication
ANDA 212493
Identifiers
- fda_app_no: ANDA212493
Properties
| Property | Value |
|---|---|
| applicant_name | AMNEAL EU LTD |
| application_type | ANDA |
| approval_date | 2023-12-08 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| DARUNAVIR | DARUNAVIR | 600MG | TABLET;ORAL |
| DARUNAVIR | DARUNAVIR | 800MG | TABLET;ORAL |
2 products