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
60505-0157-1	60505-0157	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20060117	N/A	ANDA	ANDA076143	Apotex Corp	BUPROPION HYDROCHLORIDE	100 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (60505-0157-1)
60505-0157-3	60505-0157	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20060117	N/A	ANDA	ANDA076143	Apotex Corp	BUPROPION HYDROCHLORIDE	100 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (60505-0157-3)
60505-0157-5	60505-0157	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20060117	N/A	ANDA	ANDA076143	Apotex Corp	BUPROPION HYDROCHLORIDE	100 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (60505-0157-5)
60505-0157-7	60505-0157	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20060117	N/A	ANDA	ANDA076143	Apotex Corp	BUPROPION HYDROCHLORIDE	100 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (60505-0157-7)
60505-0157-9	60505-0157	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20060117	N/A	ANDA	ANDA076143	Apotex Corp	BUPROPION HYDROCHLORIDE	100 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (60505-0157-9)
60505-0158-1	60505-0158	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20060117	N/A	ANDA	ANDA076143	Apotex Corp	BUPROPION HYDROCHLORIDE	75 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (60505-0158-1)
60505-0158-3	60505-0158	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20060117	N/A	ANDA	ANDA076143	Apotex Corp	BUPROPION HYDROCHLORIDE	75 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (60505-0158-3)
60505-0158-5	60505-0158	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20060117	N/A	ANDA	ANDA076143	Apotex Corp	BUPROPION HYDROCHLORIDE	75 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (60505-0158-5)
60505-0158-7	60505-0158	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20060117	N/A	ANDA	ANDA076143	Apotex Corp	BUPROPION HYDROCHLORIDE	75 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (60505-0158-7)
60505-0158-9	60505-0158	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20060117	N/A	ANDA	ANDA076143	Apotex Corp	BUPROPION HYDROCHLORIDE	75 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (60505-0158-9)
0904-6635-61	0904-6635	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20060117	N/A	ANDA	ANDA076143	Major Pharmaceuticals	BUPROPION HYDROCHLORIDE	75 mg/1	100 BLISTER PACK in 1 CARTON (0904-6635-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK
0904-6636-61	0904-6636	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20060117	N/A	ANDA	ANDA076143	Major Pharmaceuticals	BUPROPION HYDROCHLORIDE	100 mg/1	100 BLISTER PACK in 1 CARTON (0904-6636-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK
55700-779-30	55700-779	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20210910	N/A	ANDA	ANDA076143	Quality Care Products, LLC	BUPROPION HYDROCHLORIDE	100 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (55700-779-30)
55700-779-60	55700-779	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20190726	N/A	ANDA	ANDA076143	Quality Care Products, LLC	BUPROPION HYDROCHLORIDE	100 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (55700-779-60)
68001-308-00	68001-308	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20170208	N/A	ANDA	ANDA076143	BluePoint Laboratories	BUPROPION HYDROCHLORIDE	75 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68001-308-00)
68001-309-00	68001-309	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20170208	N/A	ANDA	ANDA076143	BluePoint Laboratories	BUPROPION HYDROCHLORIDE	100 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68001-309-00)
70518-1566-0	70518-1566	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20181022	N/A	ANDA	ANDA076143	REMEDYREPACK INC.	BUPROPION HYDROCHLORIDE	75 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1566-0)
70518-1584-0	70518-1584	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20181024	N/A	ANDA	ANDA076143	REMEDYREPACK INC.	BUPROPION HYDROCHLORIDE	100 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1584-0)
70518-1584-1	70518-1584	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20190219	N/A	ANDA	ANDA076143	REMEDYREPACK INC.	BUPROPION HYDROCHLORIDE	100 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1584-1)
60687-340-01	60687-340	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20180129	N/A	ANDA	ANDA076143	American Health Packaging	BUPROPION HYDROCHLORIDE	75 mg/1	100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-340-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-340-11)