# Benazepril Hydrochloride

NDC: 43547-337
Generic name: Benazepril Hydrochloride
Labeler / Manufacturer: Solco healthcare U.S., LLC
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:"43547-337"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43547-337
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=bb91223e-ffa5-4a3a-b191-fe121250c20c