FdaApplication
ANDA 211080
Identifiers
- fda_app_no: ANDA211080
Properties
| Property | Value |
|---|---|
| applicant_name | PRINSTON PHARMACEUTICAL INC |
| application_type | ANDA |
| approval_date | 2018-08-28 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| FENOFIBRATE | FENOFIBRATE | 48MG | TABLET;ORAL |
| FENOFIBRATE | FENOFIBRATE | 145MG | TABLET;ORAL |
2 products