FdaApplication
ANDA 203162
Identifiers
- fda_app_no: ANDA203162
Properties
| Property | Value |
|---|---|
| applicant_name | ZYDUS PHARMACEUTICALS USA INC |
| application_type | ANDA |
| approval_date | 2017-08-31 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| DONEPEZIL HYDROCHLORIDE | DONEPEZIL HYDROCHLORIDE | 23MG | TABLET;ORAL |
1 product