FdaApplication
ANDA 071969
Identifiers
- fda_app_no: ANDA071969
Properties
| Property | Value |
|---|---|
| applicant_name | WATSON LABORATORIES INC |
| application_type | ANDA |
| approval_date | 1988-04-17 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| TRIAMTERENE AND HYDROCHLOROTHIAZIDE | HYDROCHLOROTHIAZIDE; TRIAMTERENE | 50MG;75MG | TABLET;ORAL |
1 product