FdaApplication
ANDA 076900
Identifiers
- fda_app_no: ANDA076900
Properties
| Property | Value |
|---|---|
| applicant_name | ZYDUS PHARMACEUTICALS USA INC |
| application_type | ANDA |
| approval_date | 2005-01-28 |
Products (3)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ATENOLOL | ATENOLOL | 50MG | TABLET;ORAL |
| ATENOLOL | ATENOLOL | 25MG | TABLET;ORAL |
| ATENOLOL | ATENOLOL | 100MG | TABLET;ORAL |
3 products