# Benazepril Hydrochloride

NDC: 50090-3359
Generic name: Benazepril Hydrochloride
Labeler / Manufacturer: A-S Medication Solutions
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20080522

FDA application: ANDA078212

## 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:"50090-3359"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50090-3359
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c5090372-41bf-4677-b198-97fd55a0cb87