FdaApplication
ANDA 213442
Identifiers
- fda_app_no: ANDA213442
Properties
| Property | Value |
|---|---|
| applicant_name | ZYDUS PHARMACEUTICALS USA INC |
| application_type | ANDA |
| approval_date | 2023-11-29 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| IVABRADINE HYDROCHLORIDE | IVABRADINE HYDROCHLORIDE | EQ 5MG BASE | TABLET;ORAL |
| IVABRADINE HYDROCHLORIDE | IVABRADINE HYDROCHLORIDE | EQ 7.5MG BASE | TABLET;ORAL |
2 products