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
0904-7036-04	0904-7036	HUMAN PRESCRIPTION DRUG	NALTREXONE HYDROCHLORIDE	NALTREXONE HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20120229	N/A	ANDA	ANDA090356	Major Pharmaceuticals	NALTREXONE HYDROCHLORIDE	50 mg/1	30 BLISTER PACK in 1 CARTON (0904-7036-04) / 1 TABLET, FILM COATED in 1 BLISTER PACK
71335-2062-1	71335-2062	HUMAN PRESCRIPTION DRUG	NALTREXONE HYDROCHLORIDE	NALTREXONE HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20220321	N/A	ANDA	ANDA090356	Bryant Ranch Prepack	NALTREXONE HYDROCHLORIDE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-2062-1)
71335-2062-2	71335-2062	HUMAN PRESCRIPTION DRUG	NALTREXONE HYDROCHLORIDE	NALTREXONE HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20220321	N/A	ANDA	ANDA090356	Bryant Ranch Prepack	NALTREXONE HYDROCHLORIDE	50 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-2062-2)
71335-2062-3	71335-2062	HUMAN PRESCRIPTION DRUG	NALTREXONE HYDROCHLORIDE	NALTREXONE HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20220321	N/A	ANDA	ANDA090356	Bryant Ranch Prepack	NALTREXONE HYDROCHLORIDE	50 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-2062-3)
71335-2062-4	71335-2062	HUMAN PRESCRIPTION DRUG	NALTREXONE HYDROCHLORIDE	NALTREXONE HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20220321	N/A	ANDA	ANDA090356	Bryant Ranch Prepack	NALTREXONE HYDROCHLORIDE	50 mg/1	45 TABLET, FILM COATED in 1 BOTTLE (71335-2062-4)
71335-2062-5	71335-2062	HUMAN PRESCRIPTION DRUG	NALTREXONE HYDROCHLORIDE	NALTREXONE HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20220321	N/A	ANDA	ANDA090356	Bryant Ranch Prepack	NALTREXONE HYDROCHLORIDE	50 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (71335-2062-5)
71335-2062-6	71335-2062	HUMAN PRESCRIPTION DRUG	NALTREXONE HYDROCHLORIDE	NALTREXONE HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20220321	N/A	ANDA	ANDA090356	Bryant Ranch Prepack	NALTREXONE HYDROCHLORIDE	50 mg/1	15 TABLET, FILM COATED in 1 BOTTLE (71335-2062-6)
47335-326-08	47335-326	HUMAN PRESCRIPTION DRUG	NALTREXONE HYDROCHLORIDE	NALTREXONE HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20120229	N/A	ANDA	ANDA090356	Sun Pharmaceutical Industries, Inc.	NALTREXONE HYDROCHLORIDE	50 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (47335-326-08)
47335-326-18	47335-326	HUMAN PRESCRIPTION DRUG	NALTREXONE HYDROCHLORIDE	NALTREXONE HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20120229	N/A	ANDA	ANDA090356	Sun Pharmaceutical Industries, Inc.	NALTREXONE HYDROCHLORIDE	50 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (47335-326-18)
47335-326-83	47335-326	HUMAN PRESCRIPTION DRUG	NALTREXONE HYDROCHLORIDE	NALTREXONE HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20120229	N/A	ANDA	ANDA090356	Sun Pharmaceutical Industries, Inc.	NALTREXONE HYDROCHLORIDE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (47335-326-83)
47335-326-88	47335-326	HUMAN PRESCRIPTION DRUG	NALTREXONE HYDROCHLORIDE	NALTREXONE HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20120229	N/A	ANDA	ANDA090356	Sun Pharmaceutical Industries, Inc.	NALTREXONE HYDROCHLORIDE	50 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (47335-326-88)