FdaApplication
ANDA 071461
Identifiers
- fda_app_no: ANDA071461
Properties
| Property | Value |
|---|---|
| applicant_name | IVAX PHARMACEUTICALS INC SUB TEVA PHARMACEUTICALS USA |
| application_type | ANDA |
| approval_date | 1988-03-08 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| METHYLDOPA AND HYDROCHLOROTHIAZIDE | HYDROCHLOROTHIAZIDE; METHYLDOPA | 50MG;500MG | TABLET;ORAL |
1 product