# Benazepril Hydrochloride

NDC: 72162-1816
Generic name: Benazepril Hydrochloride
Labeler / Manufacturer: Bryant Ranch Prepack
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20100202

FDA application: ANDA076820

## 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:"72162-1816"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72162-1816
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=449e89a3-7bef-44eb-8d73-c77ece611cce