Package 71335-1480-6
Brand: naltrexone hydrochloride
Generic: naltrexone hydrochloridePackage Facts
Identity
Package NDC
71335-1480-6
Digits Only
7133514806
Product NDC
71335-1480
Description
15 TABLET, FILM COATED in 1 BOTTLE (71335-1480-6)
Marketing
Marketing Status
Brand
naltrexone hydrochloride
Generic
naltrexone hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "63da50ae-3486-4314-bbfd-dd0ba473bfdc", "openfda": {"unii": ["Z6375YW9SF"], "rxcui": ["1483744"], "spl_set_id": ["838a1e88-1179-4a2a-a737-8ce008bb96a7"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-1480-1)", "package_ndc": "71335-1480-1", "marketing_start_date": "20200116"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-1480-2)", "package_ndc": "71335-1480-2", "marketing_start_date": "20200122"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-1480-3)", "package_ndc": "71335-1480-3", "marketing_start_date": "20240530"}, {"sample": false, "description": "45 TABLET, FILM COATED in 1 BOTTLE (71335-1480-4)", "package_ndc": "71335-1480-4", "marketing_start_date": "20240530"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (71335-1480-5)", "package_ndc": "71335-1480-5", "marketing_start_date": "20240530"}, {"sample": false, "description": "15 TABLET, FILM COATED in 1 BOTTLE (71335-1480-6)", "package_ndc": "71335-1480-6", "marketing_start_date": "20200910"}], "brand_name": "NALTREXONE HYDROCHLORIDE", "product_id": "71335-1480_63da50ae-3486-4314-bbfd-dd0ba473bfdc", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "71335-1480", "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"}