FdaApplication
ANDA 071771
Identifiers
- fda_app_no: ANDA071771
Properties
| Property | Value |
|---|---|
| applicant_name | WARNER CHILCOTT DIV WARNER LAMBERT CO |
| application_type | ANDA |
| approval_date | 1988-01-26 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PROPRANOLOL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE | HYDROCHLOROTHIAZIDE; PROPRANOLOL HYDROCHLORIDE | 25MG;40MG | TABLET;ORAL |
1 product