FdaApplication
ANDA 203500
Identifiers
- fda_app_no: ANDA203500
Properties
| Property | Value |
|---|---|
| applicant_name | DR REDDYS LABORATORIES LTD |
| application_type | ANDA |
| approval_date | 2012-09-27 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| IRBESARTAN AND HYDROCHLOROTHIAZIDE | HYDROCHLOROTHIAZIDE; IRBESARTAN | 12.5MG;300MG | TABLET;ORAL |
| IRBESARTAN AND HYDROCHLOROTHIAZIDE | HYDROCHLOROTHIAZIDE; IRBESARTAN | 12.5MG;150MG | TABLET;ORAL |
2 products