FdaApplication
ANDA 204293
Identifiers
- fda_app_no: ANDA204293
Properties
| Property | Value |
|---|---|
| applicant_name | SUN PHARMACEUTICAL INDUSTRIES LTD |
| application_type | ANDA |
| approval_date | 2015-06-05 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| DONEPEZIL HYDROCHLORIDE | DONEPEZIL HYDROCHLORIDE | 23MG | TABLET;ORAL |
1 product