美国药品NDC（国家药品编码）与药品说明书数据库（U.S. FDA National Drug Code DataBase）

NDC包装代码	产品NDC	产品类型	商品名	通用名	剂型	给药途径	上市日期	结束日期	市场类别	申请号	标签持有者	活性成分	规格	包装描述
71335-1480-4	71335-1480	HUMAN PRESCRIPTION DRUG	NALTREXONE HYDROCHLORIDE	naltrexone hydrochloride	TABLET, FILM COATED	ORAL	20240530	N/A	ANDA	ANDA076264	Bryant Ranch Prepack	NALTREXONE HYDROCHLORIDE	50 mg/1	45 TABLET, FILM COATED in 1 BOTTLE (71335-1480-4)
71335-1480-5	71335-1480	HUMAN PRESCRIPTION DRUG	NALTREXONE HYDROCHLORIDE	naltrexone hydrochloride	TABLET, FILM COATED	ORAL	20240530	N/A	ANDA	ANDA076264	Bryant Ranch Prepack	NALTREXONE HYDROCHLORIDE	50 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (71335-1480-5)
71335-1480-3	71335-1480	HUMAN PRESCRIPTION DRUG	NALTREXONE HYDROCHLORIDE	naltrexone hydrochloride	TABLET, FILM COATED	ORAL	20240530	N/A	ANDA	ANDA076264	Bryant Ranch Prepack	NALTREXONE HYDROCHLORIDE	50 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-1480-3)
71335-1480-2	71335-1480	HUMAN PRESCRIPTION DRUG	NALTREXONE HYDROCHLORIDE	naltrexone hydrochloride	TABLET, FILM COATED	ORAL	20200122	N/A	ANDA	ANDA076264	Bryant Ranch Prepack	NALTREXONE HYDROCHLORIDE	50 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-1480-2)
71335-1480-1	71335-1480	HUMAN PRESCRIPTION DRUG	NALTREXONE HYDROCHLORIDE	naltrexone hydrochloride	TABLET, FILM COATED	ORAL	20200116	N/A	ANDA	ANDA076264	Bryant Ranch Prepack	NALTREXONE HYDROCHLORIDE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-1480-1)
71335-1480-6	71335-1480	HUMAN PRESCRIPTION DRUG	NALTREXONE HYDROCHLORIDE	naltrexone hydrochloride	TABLET, FILM COATED	ORAL	20200910	N/A	ANDA	ANDA076264	Bryant Ranch Prepack	NALTREXONE HYDROCHLORIDE	50 mg/1	15 TABLET, FILM COATED in 1 BOTTLE (71335-1480-6)
0406-1170-01	0406-1170	HUMAN PRESCRIPTION DRUG	NALTREXONE HYDROCHLORIDE	naltrexone hydrochloride	TABLET, FILM COATED	ORAL	20020322	N/A	ANDA	ANDA076264	SpecGx LLC	NALTREXONE HYDROCHLORIDE	50 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (0406-1170-01)
0406-1170-03	0406-1170	HUMAN PRESCRIPTION DRUG	NALTREXONE HYDROCHLORIDE	naltrexone hydrochloride	TABLET, FILM COATED	ORAL	20020322	N/A	ANDA	ANDA076264	SpecGx LLC	NALTREXONE HYDROCHLORIDE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0406-1170-03)
72162-2154-3	72162-2154	HUMAN PRESCRIPTION DRUG	NALTREXONE HYDROCHLORIDE	naltrexone hydrochloride	TABLET, FILM COATED	ORAL	20231207	N/A	ANDA	ANDA076264	Bryant Ranch Prepack	NALTREXONE HYDROCHLORIDE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (72162-2154-3)
68084-291-21	68084-291	HUMAN PRESCRIPTION DRUG	NALTREXONE HYDROCHLORIDE	naltrexone hydrochloride	TABLET, FILM COATED	ORAL	20130603	N/A	ANDA	ANDA076264	American Health Packaging	NALTREXONE HYDROCHLORIDE	50 mg/1	30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-291-21) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-291-11)
50090-6820-0	50090-6820	HUMAN PRESCRIPTION DRUG	NALTREXONE HYDROCHLORIDE	naltrexone hydrochloride	TABLET, FILM COATED	ORAL	20231114	N/A	ANDA	ANDA076264	A-S Medication Solutions	NALTREXONE HYDROCHLORIDE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (50090-6820-0)