FdaApplication
ANDA 076739
Identifiers
- fda_app_no: ANDA076739
Properties
| Property | Value |
|---|---|
| applicant_name | SUN PHARMACEUTICAL INDUSTRIES LTD |
| application_type | ANDA |
| approval_date | 2004-12-17 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| FOSINOPRIL SODIUM AND HYDROCHLOROTHIAZIDE | FOSINOPRIL SODIUM; HYDROCHLOROTHIAZIDE | 20MG;12.5MG | TABLET;ORAL |
| FOSINOPRIL SODIUM AND HYDROCHLOROTHIAZIDE | FOSINOPRIL SODIUM; HYDROCHLOROTHIAZIDE | 10MG;12.5MG | TABLET;ORAL |
2 products