# Moexipril Hydrochloride

NDC: 62135-967
Generic name: Moexipril Hydrochloride
Labeler / Manufacturer: Chartwell RX, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20061130

FDA application: ANDA077536

## Active ingredients

- MOEXIPRIL HYDROCHLORIDE: 7.5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"62135-967"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=62135-967
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=5c24072c-9769-4cb5-b8da-bf814d21391d