Package 51407-959-30

Brand: naltrexone hydrochloride

Generic: naltrexone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51407-959-30
Digits Only 5140795930
Product NDC 51407-959
Description

30 TABLET, FILM COATED in 1 BOTTLE (51407-959-30)

Marketing

Marketing Status
Marketed Since 2025-06-11
Brand naltrexone hydrochloride
Generic naltrexone hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3cbd097c-11db-6e77-e063-6294a90a3c7b", "openfda": {"unii": ["Z6375YW9SF"], "rxcui": ["1483744"], "spl_set_id": ["3cbd0cad-7c56-ac0a-e063-6294a90a80e4"], "manufacturer_name": ["Golden State Medical Supply, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (51407-959-01)", "package_ndc": "51407-959-01", "marketing_start_date": "20250611"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (51407-959-30)", "package_ndc": "51407-959-30", "marketing_start_date": "20250611"}], "brand_name": "NALTREXONE HYDROCHLORIDE", "product_id": "51407-959_3cbd097c-11db-6e77-e063-6294a90a3c7b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "51407-959", "generic_name": "naltrexone hydrochloride", "labeler_name": "Golden State Medical Supply, Inc.", "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"}