FdaApplication
ANDA 209951
Identifiers
- fda_app_no: ANDA209951
Properties
| Property | Value |
|---|---|
| applicant_name | AMNEAL PHARMACEUTICALS LLC |
| application_type | ANDA |
| approval_date | 2018-02-09 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| FENOFIBRATE | FENOFIBRATE | 48MG | TABLET;ORAL |
| FENOFIBRATE | FENOFIBRATE | 145MG | TABLET;ORAL |
2 products