FdaApplication
ANDA 076635
Identifiers
- fda_app_no: ANDA076635
Properties
| Property | Value |
|---|---|
| applicant_name | SUN PHARMACEUTICAL INDUSTRIES LTD |
| application_type | ANDA |
| approval_date | 2005-10-31 |
Products (3)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| FENOFIBRATE | FENOFIBRATE | 160MG | TABLET;ORAL |
| FENOFIBRATE | FENOFIBRATE | 107MG | TABLET;ORAL |
| FENOFIBRATE | FENOFIBRATE | 54MG | TABLET;ORAL |
3 products