Package 72162-2154-3

Brand: naltrexone hydrochloride

Generic: naltrexone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-2154-3
Digits Only 7216221543
Product NDC 72162-2154
Product ID 72162-2154_ba53c1a1-0bc1-444f-9dc8-fbd07df724d0
Description

30 TABLET, FILM COATED in 1 BOTTLE (72162-2154-3)

Marketing

Marketing Status
Marketed Since 2023-12-07
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": "ba53c1a1-0bc1-444f-9dc8-fbd07df724d0", "openfda": {"unii": ["Z6375YW9SF"], "rxcui": ["1483744"], "spl_set_id": ["10261f2f-e4c1-415c-b722-edeaab97a112"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72162-2154-3)", "package_ndc": "72162-2154-3", "marketing_start_date": "20231207"}], "brand_name": "NALTREXONE HYDROCHLORIDE", "product_id": "72162-2154_ba53c1a1-0bc1-444f-9dc8-fbd07df724d0", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "72162-2154", "generic_name": "naltrexone hydrochloride", "labeler_name": "Bryant Ranch Prepack", "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"}