# Benazepril hydrochloride

NDC: 62135-720
Generic name: Benazepril hydrochloride
Labeler / Manufacturer: Chartwell RX, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20220820

FDA application: ANDA076267

## 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:"62135-720"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=62135-720
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=df13d8d8-0d70-4d6f-9dd1-5da38fbe2562