# Benazepril Hydrochloride and Hydrochlorothiazide

NDC: 68462-577
Generic name: Benazepril Hydrochloride and Hydrochlorothiazide
Labeler / Manufacturer: Glenmark Pharmaceuticals Inc., USA
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20140404

FDA application: ANDA076631

## Active ingredients

- BENAZEPRIL HYDROCHLORIDE: 10 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:"68462-577"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68462-577
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=51b0aed8-a229-4d2c-8fdf-aa957fddc41b