FdaApplication
ANDA 077620
Identifiers
- fda_app_no: ANDA077620
Properties
| Property | Value |
|---|---|
| applicant_name | SUN PHARMACEUTICAL INDUSTRIES INC |
| application_type | ANDA |
| approval_date | 2008-01-11 |
Products (3)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| GLIPIZIDE AND METFORMIN HYDROCHLORIDE | GLIPIZIDE; METFORMIN HYDROCHLORIDE | 2.5MG;500MG | TABLET;ORAL |
| GLIPIZIDE AND METFORMIN HYDROCHLORIDE | GLIPIZIDE; METFORMIN HYDROCHLORIDE | 5MG;500MG | TABLET;ORAL |
| GLIPIZIDE AND METFORMIN HYDROCHLORIDE | GLIPIZIDE; METFORMIN HYDROCHLORIDE | 2.5MG;250MG | TABLET;ORAL |
3 products