# Lotensin HCT

NDC: 30698-453
Generic name: benazepril hydrochloride and hydrochlorothiazide
Labeler / Manufacturer: Validus Pharmaceuticals LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET
Routes: ORAL
Marketing started: 19920530

FDA application: NDA020033

## Active ingredients

- BENAZEPRIL HYDROCHLORIDE: 20 mg/1
- HYDROCHLOROTHIAZIDE: 12.5 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"30698-453"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=30698-453
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=94c4536f-e28e-48b1-8336-b3939917e99d