FdaApplication
ANDA 071501
Identifiers
- fda_app_no: ANDA071501
Properties
| Property | Value |
|---|---|
| applicant_name | WATSON LABORATORIES INC |
| application_type | ANDA |
| approval_date | 1991-12-18 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PROPRANOLOL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE | HYDROCHLOROTHIAZIDE; PROPRANOLOL HYDROCHLORIDE | 25MG;80MG | TABLET;ORAL |
1 product