Package 71610-964-31

Brand: naltrexone hydrochloride

Generic: naltrexone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71610-964-31
Digits Only 7161096431
Product NDC 71610-964
Product ID 71610-964_43cd684b-f17f-80ab-e063-6294a90a6f5a
Description

600 TABLET, FILM COATED in 1 BOTTLE (71610-964-31)

Marketing

Marketing Status
Marketed Since 2025-11-13
Brand naltrexone hydrochloride
Generic naltrexone hydrochloride
Sample Package No

Linked Drug Pages (1)

NALTREXONE HYDROCHLORIDE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "43cd684b-f17f-80ab-e063-6294a90a6f5a", "openfda": {"unii": ["Z6375YW9SF"], "rxcui": ["1483744"], "spl_set_id": ["43cd6961-4793-85ee-e063-6294a90ad772"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "600 TABLET, FILM COATED in 1 BOTTLE (71610-964-31)", "package_ndc": "71610-964-31", "marketing_start_date": "20251113"}], "brand_name": "NALTREXONE HYDROCHLORIDE", "product_id": "71610-964_43cd684b-f17f-80ab-e063-6294a90a6f5a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "71610-964", "generic_name": "naltrexone hydrochloride", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "NALTREXONE HYDROCHLORIDE", "active_ingredients": [{"name": "NALTREXONE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA076264", "marketing_category": "ANDA", "marketing_start_date": "20020322", "listing_expiration_date": "20261231"}