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
71610-708-80	71610-708	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20230516	N/A	ANDA	ANDA076143	Aphena Pharma Solutions - Tennessee, LLC	BUPROPION HYDROCHLORIDE	100 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (71610-708-80)
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)
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)
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)
72789-070-30	72789-070	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20200326	N/A	ANDA	ANDA076143	PD-Rx Pharmaceuticals, Inc.	BUPROPION HYDROCHLORIDE	100 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-070-30)
71610-774-53	71610-774	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20240122	N/A	ANDA	ANDA076143	Aphena Pharma Solutions - Tennessee, LLC	BUPROPION HYDROCHLORIDE	75 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71610-774-53)
71610-774-70	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	120 TABLET, FILM COATED in 1 BOTTLE (71610-774-70)
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)
45865-473-30	45865-473	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20210908	N/A	ANDA	ANDA076143	Medsource Pharmaceuticals	BUPROPION HYDROCHLORIDE	75 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (45865-473-30)
68071-2577-3	68071-2577	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20211117	N/A	ANDA	ANDA076143	NuCare Pharmaceuticals,Inc.	BUPROPION HYDROCHLORIDE	100 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68071-2577-3)
55154-8180-0	55154-8180	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20180129	N/A	ANDA	ANDA076143	Cardinal Health 107, LLC	BUPROPION HYDROCHLORIDE	75 mg/1	10 BLISTER PACK in 1 BAG (55154-8180-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
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)