FdaApplication
ANDA 208332
Identifiers
- fda_app_no: ANDA208332
Properties
| Property | Value |
|---|---|
| applicant_name | APOTEX INC |
| application_type | ANDA |
| approval_date | 2017-06-12 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| EZETIMIBE | EZETIMIBE | 10MG | TABLET;ORAL |
1 product