FdaApplication
ANDA 202900
Identifiers
- fda_app_no: ANDA202900
Properties
| Property | Value |
|---|---|
| applicant_name | ZYDUS PHARMACEUTICALS USA INC |
| application_type | ANDA |
| approval_date | 2018-04-30 |
Products (3)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| BUMETANIDE | BUMETANIDE | 1MG | TABLET;ORAL |
| BUMETANIDE | BUMETANIDE | 2MG | TABLET;ORAL |
| BUMETANIDE | BUMETANIDE | 0.5MG | TABLET;ORAL |
3 products