# NALTREXONE HYDROCHLORIDE

NDC: 68084-291
Generic name: naltrexone hydrochloride
Labeler / Manufacturer: American Health Packaging
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20130603

FDA application: ANDA076264

## 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:"68084-291"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68084-291
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=81e25c6a-81b6-4cfb-91bf-be20c3ae546b