# Naltrexone Hydrochloride

NDC: 70518-4344
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: 20250520

FDA application: ANDA075274

## 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:"70518-4344"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70518-4344
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=db911559-26f5-43a0-b61f-3425176c936f