FdaApplication
ANDA 212931
Identifiers
- fda_app_no: ANDA212931
Properties
| Property | Value |
|---|---|
| applicant_name | APPCO PHARMA LLC |
| application_type | ANDA |
| approval_date | 2024-09-18 |
Products (3)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| BUMETANIDE | BUMETANIDE | 0.5MG | TABLET;ORAL |
| BUMETANIDE | BUMETANIDE | 2MG | TABLET;ORAL |
| BUMETANIDE | BUMETANIDE | 1MG | TABLET;ORAL |
3 products