# Quinapril

NDC: 65862-617
Generic name: Quinapril Hydrochloride
Labeler / Manufacturer: Aurobindo Pharma Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20130429

FDA application: ANDA202725

## Active ingredients

- QUINAPRIL HYDROCHLORIDE: 5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"65862-617"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=65862-617
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=93e6e668-5306-4f26-81d8-cbc3a7a5e787