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
60505-0157-5	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)
82804-127-30	82804-127	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20240718	N/A	ANDA	ANDA076143	Proficient Rx LP	BUPROPION HYDROCHLORIDE	75 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (82804-127-30)
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)
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)