# Benazepril Hydrochloride

NDC: 70518-4633
Generic name: Benazepril Hydrochloride
Labeler / Manufacturer: REMEDYREPACK INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20260425

FDA application: ANDA076267

## 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:"70518-4633"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70518-4633
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6dc12ab4-2282-412f-8aa1-46ec5fbbab8f