FdaApplication
ANDA 208832
Identifiers
- fda_app_no: ANDA208832
Properties
| Property | Value |
|---|---|
| applicant_name | AMNEAL PHARMACEUTICALS CO GMBH |
| application_type | ANDA |
| approval_date | 2017-06-02 |
Products (3)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| NADOLOL | NADOLOL | 40MG | TABLET;ORAL |
| NADOLOL | NADOLOL | 80MG | TABLET;ORAL |
| NADOLOL | NADOLOL | 20MG | TABLET;ORAL |
3 products