# Benazepril Hydrochloride and Hydrochlorothiazide

NDC: 0185-0211
Generic name: Benazepril Hydrochloride and Hydrochlorothiazide
Labeler / Manufacturer: Sandoz Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20040211

FDA application: ANDA076631

## Active ingredients

- BENAZEPRIL HYDROCHLORIDE: 20 mg/1
- HYDROCHLOROTHIAZIDE: 12.5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0185-0211"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0185-0211
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c9bdfbb4-87b6-4de4-bc1d-5025d3ef591f