FdaApplication
ANDA 201748
Identifiers
- fda_app_no: ANDA201748
Properties
| Property | Value |
|---|---|
| applicant_name | SUN PHARMACEUTICAL INDUSTRIES LTD |
| application_type | ANDA |
| approval_date | 2014-10-31 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| FENOFIBRATE (MICRONIZED) | FENOFIBRATE | 43MG | CAPSULE;ORAL |
| FENOFIBRATE (MICRONIZED) | FENOFIBRATE | 130MG | CAPSULE;ORAL |
2 products