# Benazepril Hydrochloride

NDC: 68071-1769
Generic name: Benazepril Hydrochloride
Labeler / Manufacturer: NuCare Pharmaceuticals,Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, COATED
Routes: ORAL
Marketing started: 20140101

FDA application: ANDA076118

## Active ingredients

- BENAZEPRIL HYDROCHLORIDE: 20 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68071-1769"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68071-1769
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9535ec77-2d50-4817-e053-2995a90a007e