# Naltrexone Hydrochloride

NDC: 67046-0060
Generic name: Naltrexone Hydrochloride
Labeler / Manufacturer: Coupler LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20260527
Marketing ended: 20271130
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:"67046-0060"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=67046-0060
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=56055980-d23b-ec7d-e063-6394a90a9cc2