FdaApplication
ANDA 076786
Identifiers
- fda_app_no: ANDA076786
Properties
| Property | Value |
|---|---|
| applicant_name | SUN PHARMACEUTICAL INDUSTRIES LTD |
| application_type | ANDA |
| approval_date | 2010-11-26 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| DONEPEZIL HYDROCHLORIDE | DONEPEZIL HYDROCHLORIDE | 5MG | TABLET;ORAL |
| DONEPEZIL HYDROCHLORIDE | DONEPEZIL HYDROCHLORIDE | 10MG | TABLET;ORAL |
2 products