Package 71610-919-31

Brand: naltrexone hydrochloride

Generic: naltrexone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71610-919-31
Digits Only 7161091931
Product NDC 71610-919
Product ID 71610-919_390beeb7-865f-e87d-e063-6394a90a8822
Description

600 TABLET, FILM COATED in 1 BOTTLE (71610-919-31)

Marketing

Marketing Status
Marketed Since 2025-07-01
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": "390beeb7-865f-e87d-e063-6394a90a8822", "openfda": {"unii": ["Z6375YW9SF"], "rxcui": ["1483744"], "spl_set_id": ["390bff41-7bab-b72a-e063-6294a90ad35d"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "600 TABLET, FILM COATED in 1 BOTTLE (71610-919-31)", "package_ndc": "71610-919-31", "marketing_start_date": "20250701"}], "brand_name": "NALTREXONE HYDROCHLORIDE", "product_id": "71610-919_390beeb7-865f-e87d-e063-6394a90a8822", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "71610-919", "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"}