FdaApplication
NDA 019851
Identifiers
- fda_app_no: NDA019851
Properties
| Property | Value |
|---|---|
| applicant_name | VALIDUS PHARMACEUTICALS LLC |
| application_type | NDA |
| approval_date | 1991-06-25 |
Products (4)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| LOTENSIN | BENAZEPRIL HYDROCHLORIDE | 20MG | TABLET;ORAL |
| LOTENSIN | BENAZEPRIL HYDROCHLORIDE | 5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
| LOTENSIN | BENAZEPRIL HYDROCHLORIDE | 10MG | TABLET;ORAL |
| LOTENSIN | BENAZEPRIL HYDROCHLORIDE | 40MG | TABLET;ORAL |
4 products