FdaApplication
NDA 018872
Identifiers
- fda_app_no: NDA018872
Properties
| Property | Value |
|---|---|
| applicant_name | NOVARTIS PHARMACEUTICALS CORP |
| application_type | NDA |
| approval_date | 1987-07-22 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| VISKAZIDE | HYDROCHLOROTHIAZIDE; PINDOLOL | 25MG;5MG | TABLET;ORAL |
| VISKAZIDE | HYDROCHLOROTHIAZIDE; PINDOLOL | 25MG;10MG | TABLET;ORAL |
2 products