Package 16729-081-10

Brand: naltrexone hydrochloride

Generic: naltrexone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 16729-081-10
Digits Only 1672908110
Product NDC 16729-081
Product ID 16729-081_424db74c-6c0f-1eb3-e063-6294a90a7db8
Description

30 TABLET, FILM COATED in 1 BOTTLE (16729-081-10)

Marketing

Marketing Status
Marketed Since 2012-01-18
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": "424db74c-6c0f-1eb3-e063-6294a90a7db8", "openfda": {"unii": ["Z6375YW9SF"], "rxcui": ["1483744"], "spl_set_id": ["49aa3d6d-2270-4615-aafa-b440859ab870"], "manufacturer_name": ["Accord Healthcare, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (16729-081-01)", "package_ndc": "16729-081-01", "marketing_start_date": "20120118"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (16729-081-10)", "package_ndc": "16729-081-10", "marketing_start_date": "20120118"}], "brand_name": "Naltrexone Hydrochloride", "product_id": "16729-081_424db74c-6c0f-1eb3-e063-6294a90a7db8", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "16729-081", "generic_name": "Naltrexone Hydrochloride", "labeler_name": "Accord Healthcare, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Naltrexone Hydrochloride", "active_ingredients": [{"name": "NALTREXONE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA091205", "marketing_category": "ANDA", "marketing_start_date": "20120118", "listing_expiration_date": "20261231"}