# BENAZEPRIL HYDROCHLORIDE

NDC: 72189-110
Generic name: BENAZEPRIL HYDROCHLORIDE
Labeler / Manufacturer: DIRECT RX
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, COATED
Routes: ORAL
Marketing started: 20200612

FDA application: ANDA076118

## 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:"72189-110"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72189-110
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a7e4e43a-7abc-e2a5-e053-2995a90ab5f4