# Lotensin

NDC: 30698-448
Generic name: benazepril hydrochloride
Labeler / Manufacturer: Validus Pharmaceuticals LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET
Routes: ORAL
Marketing started: 19910621

FDA application: NDA019851

## Active ingredients

- BENAZEPRIL HYDROCHLORIDE: 10 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"30698-448"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=30698-448
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2abb091b-a53e-46b0-9b84-e5ee8f2bdd8e