# Quinapril and Hydrochlorothiazide

NDC: 62135-669
Generic name: Quinapril and Hydrochlorothiazide
Labeler / Manufacturer: Chartwell RX, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20040331

FDA application: ANDA076374

## Active ingredients

- HYDROCHLOROTHIAZIDE: 25 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:"62135-669"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=62135-669
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2eae533f-d0af-47e8-a1f2-94bc8cc89b5a