FdaApplication
ANDA 202252
Identifiers
- fda_app_no: ANDA202252
Properties
| Property | Value |
|---|---|
| applicant_name | APOTEX INC |
| application_type | ANDA |
| approval_date | 2013-07-26 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| FENOFIBRATE (MICRONIZED) | FENOFIBRATE | 43MG | CAPSULE;ORAL |
| FENOFIBRATE (MICRONIZED) | FENOFIBRATE | 130MG | CAPSULE;ORAL |
2 products