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
71610-774-80	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)
72162-2098-1	72162-2098	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20060117	N/A	ANDA	ANDA076143	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	75 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (72162-2098-1)