FdaApplication
ANDA 207805
Identifiers
- fda_app_no: ANDA207805
Properties
| Property | Value |
|---|---|
| applicant_name | REYOUNG CORPORATION |
| application_type | ANDA |
| approval_date | 2017-11-16 |
Products (3)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| FENOFIBRATE (MICRONIZED) | FENOFIBRATE | 67MG | CAPSULE;ORAL |
| FENOFIBRATE (MICRONIZED) | FENOFIBRATE | 200MG | CAPSULE;ORAL |
| FENOFIBRATE (MICRONIZED) | FENOFIBRATE | 134MG | CAPSULE;ORAL |
3 products