FdaApplication
ANDA 210859
Identifiers
- fda_app_no: ANDA210859
Properties
| Property | Value |
|---|---|
| applicant_name | HETERO LABS LTD UNIT III |
| application_type | ANDA |
| approval_date | 2022-07-26 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| EZETIMIBE | EZETIMIBE | 10MG | TABLET;ORAL |
1 product