LOTENSIN (BENAZEPRIL HYDROCHLORIDE) — FDA Approval NDA019851 (VALIDUS PHARMS)
LOTENSIN (BENAZEPRIL HYDROCHLORIDE) — FDA Approval NDA019851 (VALIDUS PHARMS) is one of 9,000 drug approvals in the DrugApprovals dataset. Key details — Brand name: LOTENSIN; Active ingredients: BENAZEPRIL HYDROCHLORIDE; Application number: NDA019851.
| Brand name | LOTENSIN |
|---|---|
| Active ingredients | BENAZEPRIL HYDROCHLORIDE |
| Application number | NDA019851 |
| Sponsor | VALIDUS PHARMS |
| Dosage form | TABLET |
| Route | ORAL |
| Marketing status | Prescription |
| Products in application | 4 |
| First approval date | 19910625 |
| Source | openFDA Drugs@FDA |
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