# Naltrexone Hydrochloride

NDC: 62135-242
Generic name: Naltrexone 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: 20170721

FDA application: ANDA207905

## Active ingredients

- NALTREXONE HYDROCHLORIDE: 50 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"62135-242"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=62135-242
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=adb7c4dc-221a-4d91-9687-0d78913a92ad