# Benazepril Hydrochloride

NDC: 50090-0914
Generic name: Benazepril Hydrochloride
Labeler / Manufacturer: A-S Medication Solutions
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: 40 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"50090-0914"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50090-0914
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8f46e2c9-9b3b-48d0-a307-9069e3879959