FdaApplication
ANDA 209660
Identifiers
- fda_app_no: ANDA209660
Properties
| Property | Value |
|---|---|
| applicant_name | CHARTWELL RX SCIENCES LLC |
| application_type | ANDA |
| approval_date | 2019-02-11 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| FENOFIBRATE | FENOFIBRATE | 54MG | TABLET;ORAL |
| FENOFIBRATE | FENOFIBRATE | 160MG | TABLET;ORAL |
2 products