Package 71335-2062-5

Brand: naltrexone hydrochloride

Generic: naltrexone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71335-2062-5
Digits Only 7133520625
Product NDC 71335-2062
Product ID 71335-2062_ab44332a-6f04-4f07-8209-e472206d5707
Description

120 TABLET, FILM COATED in 1 BOTTLE (71335-2062-5)

Marketing

Marketing Status
Marketed Since 2022-03-21
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": "ab44332a-6f04-4f07-8209-e472206d5707", "openfda": {"unii": ["Z6375YW9SF"], "rxcui": ["1483744"], "spl_set_id": ["f9807ec0-3504-4c66-8efe-ea25f84c782b"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-2062-1)", "package_ndc": "71335-2062-1", "marketing_start_date": "20220321"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-2062-2)", "package_ndc": "71335-2062-2", "marketing_start_date": "20220321"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-2062-3)", "package_ndc": "71335-2062-3", "marketing_start_date": "20220321"}, {"sample": false, "description": "45 TABLET, FILM COATED in 1 BOTTLE (71335-2062-4)", "package_ndc": "71335-2062-4", "marketing_start_date": "20220321"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (71335-2062-5)", "package_ndc": "71335-2062-5", "marketing_start_date": "20220321"}, {"sample": false, "description": "15 TABLET, FILM COATED in 1 BOTTLE (71335-2062-6)", "package_ndc": "71335-2062-6", "marketing_start_date": "20220321"}], "brand_name": "NALTREXONE HYDROCHLORIDE", "product_id": "71335-2062_ab44332a-6f04-4f07-8209-e472206d5707", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "71335-2062", "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": "ANDA090356", "marketing_category": "ANDA", "marketing_start_date": "20120229", "listing_expiration_date": "20261231"}