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
43063-880-30	43063-880	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20180813	N/A	ANDA	ANDA076143	PD-Rx Pharmaceuticals, Inc.	BUPROPION HYDROCHLORIDE	75 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-880-30)
43063-880-60	43063-880	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20181030	N/A	ANDA	ANDA076143	PD-Rx Pharmaceuticals, Inc.	BUPROPION HYDROCHLORIDE	75 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-880-60)
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)
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)
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)
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
60687-351-01	60687-351	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20180201	N/A	ANDA	ANDA076143	American Health Packaging	BUPROPION HYDROCHLORIDE	100 mg/1	100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-351-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-351-11)
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)
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)
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)