FdaApplication
ANDA 209950
Identifiers
- fda_app_no: ANDA209950
Properties
| Property | Value |
|---|---|
| applicant_name | AMNEAL PHARMACEUTICALS LLC |
| application_type | ANDA |
| approval_date | 2018-03-19 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| FENOFIBRATE | FENOFIBRATE | 160MG | TABLET;ORAL |
| FENOFIBRATE | FENOFIBRATE | 54MG | TABLET;ORAL |
2 products