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
70518-1146-1	70518-1146	HUMAN PRESCRIPTION DRUG	Naltrexone Hydrochloride	Naltrexone Hydrochloride	TABLET, FILM COATED	ORAL	20240527	N/A	ANDA	ANDA091205	REMEDYREPACK INC.	NALTREXONE HYDROCHLORIDE	50 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1146-1)
71335-0014-3	71335-0014	HUMAN PRESCRIPTION DRUG	Naltrexone Hydrochloride	Naltrexone Hydrochloride	TABLET, FILM COATED	ORAL	20170808	N/A	ANDA	ANDA091205	Bryant Ranch Prepack	NALTREXONE HYDROCHLORIDE	50 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-0014-3)
71335-0014-5	71335-0014	HUMAN PRESCRIPTION DRUG	Naltrexone Hydrochloride	Naltrexone Hydrochloride	TABLET, FILM COATED	ORAL	20170808	N/A	ANDA	ANDA091205	Bryant Ranch Prepack	NALTREXONE HYDROCHLORIDE	50 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (71335-0014-5)
71335-0014-6	71335-0014	HUMAN PRESCRIPTION DRUG	Naltrexone Hydrochloride	Naltrexone Hydrochloride	TABLET, FILM COATED	ORAL	20170808	N/A	ANDA	ANDA091205	Bryant Ranch Prepack	NALTREXONE HYDROCHLORIDE	50 mg/1	15 TABLET, FILM COATED in 1 BOTTLE (71335-0014-6)
71335-0014-2	71335-0014	HUMAN PRESCRIPTION DRUG	Naltrexone Hydrochloride	Naltrexone Hydrochloride	TABLET, FILM COATED	ORAL	20170808	N/A	ANDA	ANDA091205	Bryant Ranch Prepack	NALTREXONE HYDROCHLORIDE	50 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-0014-2)
71335-0014-1	71335-0014	HUMAN PRESCRIPTION DRUG	Naltrexone Hydrochloride	Naltrexone Hydrochloride	TABLET, FILM COATED	ORAL	20170808	N/A	ANDA	ANDA091205	Bryant Ranch Prepack	NALTREXONE HYDROCHLORIDE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-0014-1)
71335-0014-4	71335-0014	HUMAN PRESCRIPTION DRUG	Naltrexone Hydrochloride	Naltrexone Hydrochloride	TABLET, FILM COATED	ORAL	20170808	N/A	ANDA	ANDA091205	Bryant Ranch Prepack	NALTREXONE HYDROCHLORIDE	50 mg/1	45 TABLET, FILM COATED in 1 BOTTLE (71335-0014-4)
50090-4925-0	50090-4925	HUMAN PRESCRIPTION DRUG	Naltrexone Hydrochloride	Naltrexone Hydrochloride	TABLET, FILM COATED	ORAL	20200220	N/A	ANDA	ANDA091205	A-S Medication Solutions	NALTREXONE HYDROCHLORIDE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (50090-4925-0)
16729-081-01	16729-081	HUMAN PRESCRIPTION DRUG	Naltrexone Hydrochloride	Naltrexone Hydrochloride	TABLET, FILM COATED	ORAL	20120118	N/A	ANDA	ANDA091205	Accord Healthcare, Inc.	NALTREXONE HYDROCHLORIDE	50 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (16729-081-01)
16729-081-10	16729-081	HUMAN PRESCRIPTION DRUG	Naltrexone Hydrochloride	Naltrexone Hydrochloride	TABLET, FILM COATED	ORAL	20120118	N/A	ANDA	ANDA091205	Accord Healthcare, Inc.	NALTREXONE HYDROCHLORIDE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (16729-081-10)
68071-2721-3	68071-2721	HUMAN PRESCRIPTION DRUG	Naltrexone Hydrochloride	Naltrexone Hydrochloride	TABLET, FILM COATED	ORAL	20220520	N/A	ANDA	ANDA091205	NuCare Pharmceuticals,Inc.	NALTREXONE HYDROCHLORIDE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68071-2721-3)