# QUINAPRIL HYDROCHLORIDE/HYDROCHLOROTHIAZIDE

NDC: 65862-162
Generic name: QUINAPRIL HYDROCHLORIDE/HYDROCHLOROTHIAZIDE
Labeler / Manufacturer: Aurobindo Pharma Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20070824

FDA application: ANDA078450

## Active ingredients

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

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"65862-162"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=65862-162
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=50a58159-9572-4445-9859-b392632597da