FdaApplication
ANDA 073334
Identifiers
- fda_app_no: ANDA073334
Properties
| Property | Value |
|---|---|
| applicant_name | WATSON LABORATORIES INC |
| application_type | ANDA |
| approval_date | 1991-07-19 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| AMILORIDE HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE | AMILORIDE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE | EQ 5MG ANHYDROUS;50MG | TABLET;ORAL |
1 product