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
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)
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)
71610-164-83	71610-164	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20180926	N/A	ANDA	ANDA076143	Aphena Pharma Solutions - Tennessee, LLC	BUPROPION HYDROCHLORIDE	100 mg/1	3600 TABLET, FILM COATED in 1 BOTTLE (71610-164-83)
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)
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)
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)
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)