Package 42291-632-30

Brand: naltrexone hydrochloride

Generic: naltrexone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 42291-632-30
Digits Only 4229163230
Product NDC 42291-632
Product ID 42291-632_4a197f32-b382-2a52-e063-6394a90ad197
Description

30 TABLET, FILM COATED in 1 BOTTLE (42291-632-30)

Marketing

Marketing Status
Discontinued 2028-06-30
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": "4a197f32-b382-2a52-e063-6394a90ad197", "openfda": {"unii": ["Z6375YW9SF"], "rxcui": ["1483744"], "spl_set_id": ["21b43dab-015c-c82f-ba6e-27da0ec12fc5"], "manufacturer_name": ["AvKARE"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (42291-632-30)", "package_ndc": "42291-632-30", "marketing_end_date": "20280630", "marketing_start_date": "20150326"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (42291-632-60)", "package_ndc": "42291-632-60", "marketing_end_date": "20280630", "marketing_start_date": "20250724"}], "brand_name": "Naltrexone Hydrochloride", "product_id": "42291-632_4a197f32-b382-2a52-e063-6394a90ad197", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "42291-632", "generic_name": "Naltrexone Hydrochloride", "labeler_name": "AvKARE", "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": "20280630", "marketing_start_date": "20150326"}