FdaApplication
ANDA 071900
Identifiers
- fda_app_no: ANDA071900
Properties
| Property | Value |
|---|---|
| applicant_name | PARKE DAVIS DIV WARNER LAMBERT CO |
| application_type | ANDA |
| approval_date | 1987-11-23 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| METHYLDOPA AND HYDROCHLOROTHIAZIDE | HYDROCHLOROTHIAZIDE; METHYLDOPA | 50MG;500MG | TABLET;ORAL |
1 product