# NALTREXONE HYDROCHLORIDE

NDC: 70518-2718
Generic name: NALTREXONE HYDROCHLORIDE
Labeler / Manufacturer: REMEDYREPACK INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20200501

FDA application: ANDA090356

## 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:"70518-2718"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70518-2718
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f821dd49-3fa7-4d33-99de-19023ff1ae65