FdaApplication
ANDA 087004
Identifiers
- fda_app_no: ANDA087004
Properties
| Property | Value |
|---|---|
| applicant_name | IVAX PHARMACEUTICALS INC |
| application_type | ANDA |
| approval_date | 1982-05-24 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| SPIRONOLACTONE W/ HYDROCHLOROTHIAZIDE | HYDROCHLOROTHIAZIDE; SPIRONOLACTONE | 25MG;25MG | TABLET;ORAL |
1 product