# NALTREXONE HYDROCHLORIDE

NDC: 71610-919
Generic name: naltrexone hydrochloride
Labeler / Manufacturer: Aphena Pharma Solutions - Tennessee, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20020322

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:"71610-919"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71610-919
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=390bff41-7bab-b72a-e063-6294a90ad35d