FdaApplication
ANDA 202415
Identifiers
- fda_app_no: ANDA202415
Properties
| Property | Value |
|---|---|
| applicant_name | ACTAVIS ELIZABETH LLC |
| application_type | ANDA |
| approval_date | 2015-12-17 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| DONEPEZIL HYDROCHLORIDE | DONEPEZIL HYDROCHLORIDE | 23MG | TABLET;ORAL |
1 product