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
60505-0157-9	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)
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
55154-4152-0	55154-4152	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20220518	N/A	ANDA	ANDA076143	Cardinal Health 107, LLC	BUPROPION HYDROCHLORIDE	75 mg/1	10 BLISTER PACK in 1 BAG (55154-4152-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
70518-1566-0	70518-1566	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20181222	N/A	ANDA	ANDA076143	REMEDYREPACK INC.	BUPROPION HYDROCHLORIDE	75 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1566-0)
60760-781-30	60760-781	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20250521	N/A	ANDA	ANDA076143	ST. MARY'S MEDICAL PARK PHARMACY	BUPROPION HYDROCHLORIDE	100 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-781-30)
71610-774-80	71610-774	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20240125	N/A	ANDA	ANDA076143	Aphena Pharma Solutions - Tennessee, LLC	BUPROPION HYDROCHLORIDE	75 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (71610-774-80)
71610-774-94	71610-774	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20240125	N/A	ANDA	ANDA076143	Aphena Pharma Solutions - Tennessee, LLC	BUPROPION HYDROCHLORIDE	75 mg/1	360 TABLET, FILM COATED in 1 BOTTLE (71610-774-94)
50090-1869-0	50090-1869	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20150610	N/A	ANDA	ANDA076143	A-S Medication Solutions	BUPROPION HYDROCHLORIDE	100 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (50090-1869-0)
50090-1869-3	50090-1869	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20150610	N/A	ANDA	ANDA076143	A-S Medication Solutions	BUPROPION HYDROCHLORIDE	100 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (50090-1869-3)
60429-747-01	60429-747	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20190822	N/A	ANDA	ANDA076143	Golden State Medical Supply, Inc.	BUPROPION HYDROCHLORIDE	100 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (60429-747-01)
68071-2256-1	68071-2256	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20200910	N/A	ANDA	ANDA076143	NuCare Pharmaceuticals,Inc.	BUPROPION HYDROCHLORIDE	75 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68071-2256-1)
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
71335-0013-1	71335-0013	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20180308	N/A	ANDA	ANDA076143	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	75 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-0013-1)
71335-0013-2	71335-0013	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20180221	N/A	ANDA	ANDA076143	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	75 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-0013-2)
72189-457-30	72189-457	HUMAN PRESCRIPTION DRUG	Bupropion HCL	Bupropion HCL	TABLET, FILM COATED	ORAL	20230330	N/A	ANDA	ANDA076143	Direct_Rx	BUPROPION HYDROCHLORIDE	100 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (72189-457-30)
71335-0013-3	71335-0013	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20240709	N/A	ANDA	ANDA076143	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	75 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-0013-3)
71335-0013-4	71335-0013	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20240709	N/A	ANDA	ANDA076143	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	75 mg/1	7 TABLET, FILM COATED in 1 BOTTLE (71335-0013-4)
71335-0013-5	71335-0013	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20240709	N/A	ANDA	ANDA076143	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	75 mg/1	14 TABLET, FILM COATED in 1 BOTTLE (71335-0013-5)
71335-0013-6	71335-0013	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20240709	N/A	ANDA	ANDA076143	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	75 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (71335-0013-6)
71335-0013-7	71335-0013	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20240709	N/A	ANDA	ANDA076143	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	75 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (71335-0013-7)