Package 51224-206-50

Brand: naltrexone hydrochloride

Generic: naltrexone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51224-206-50
Digits Only 5122420650
Product NDC 51224-206
Product ID 51224-206_75a00517-674b-4e87-b37b-598486aedf03
Description

100 TABLET, FILM COATED in 1 BOTTLE (51224-206-50)

Marketing

Marketing Status
Discontinued 2027-11-30
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": "75a00517-674b-4e87-b37b-598486aedf03", "openfda": {"unii": ["Z6375YW9SF"], "rxcui": ["1483744"], "spl_set_id": ["60276f5c-657a-4b60-bcd0-44234903d7e0"], "manufacturer_name": ["TAGI Pharma Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (51224-206-30)", "package_ndc": "51224-206-30", "marketing_end_date": "20271130", "marketing_start_date": "20130923"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (51224-206-50)", "package_ndc": "51224-206-50", "marketing_end_date": "20271130", "marketing_start_date": "20130923"}], "brand_name": "Naltrexone Hydrochloride", "product_id": "51224-206_75a00517-674b-4e87-b37b-598486aedf03", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "51224-206", "generic_name": "Naltrexone Hydrochloride", "labeler_name": "TAGI Pharma Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Naltrexone Hydrochloride", "active_ingredients": [{"name": "NALTREXONE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA075274", "marketing_category": "ANDA", "marketing_end_date": "20271130", "marketing_start_date": "20130923"}