FdaApplication
ANDA 210577
Identifiers
- fda_app_no: ANDA210577
Properties
| Property | Value |
|---|---|
| applicant_name | AMNEAL PHARMACEUTICALS CO GMBH |
| application_type | ANDA |
| approval_date | 2018-05-15 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| HYDROXYCHLOROQUINE SULFATE | HYDROXYCHLOROQUINE SULFATE | 200MG | TABLET;ORAL |
1 product