FdaApplication
ANDA 077975
Identifiers
- fda_app_no: ANDA077975
Properties
| Property | Value |
|---|---|
| applicant_name | SUN PHARMACEUTICAL INDUSTRIES INC |
| application_type | ANDA |
| approval_date | 2009-12-11 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| DONEPEZIL HYDROCHLORIDE | DONEPEZIL HYDROCHLORIDE | 10MG | TABLET, ORALLY DISINTEGRATING;ORAL |
| DONEPEZIL HYDROCHLORIDE | DONEPEZIL HYDROCHLORIDE | 5MG | TABLET, ORALLY DISINTEGRATING;ORAL |
2 products