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
43547-290-06	43547-290	HUMAN PRESCRIPTION DRUG	bupropion hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20141101	N/A	ANDA	ANDA202304	Solco Healthcare US LLC	BUPROPION HYDROCHLORIDE	200 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (43547-290-06)
43547-290-09	43547-290	HUMAN PRESCRIPTION DRUG	bupropion hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20141101	N/A	ANDA	ANDA202304	Solco Healthcare US LLC	BUPROPION HYDROCHLORIDE	200 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (43547-290-09)
43547-290-10	43547-290	HUMAN PRESCRIPTION DRUG	bupropion hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20141101	N/A	ANDA	ANDA202304	Solco Healthcare US LLC	BUPROPION HYDROCHLORIDE	200 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (43547-290-10)
43547-290-50	43547-290	HUMAN PRESCRIPTION DRUG	bupropion hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20141101	N/A	ANDA	ANDA202304	Solco Healthcare US LLC	BUPROPION HYDROCHLORIDE	200 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (43547-290-50)
70518-4591-0	70518-4591	HUMAN PRESCRIPTION DRUG	bupropion hydrochloride SR	Bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20260320	N/A	ANDA	ANDA202304	REMEDYREPACK INC.	BUPROPION HYDROCHLORIDE	100 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-4591-0)
0904-7465-61	0904-7465	HUMAN PRESCRIPTION DRUG	bupropion hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20241115	N/A	ANDA	ANDA202304	Major Pharmaceuticals	BUPROPION HYDROCHLORIDE	150 mg/1	100 BLISTER PACK in 1 CARTON (0904-7465-61) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
43547-288-06	43547-288	HUMAN PRESCRIPTION DRUG	bupropion hydrochloride SR	Bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20141101	N/A	ANDA	ANDA202304	Solco Healthcare US LLC	BUPROPION HYDROCHLORIDE	100 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (43547-288-06)
43547-288-09	43547-288	HUMAN PRESCRIPTION DRUG	bupropion hydrochloride SR	Bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20141101	N/A	ANDA	ANDA202304	Solco Healthcare US LLC	BUPROPION HYDROCHLORIDE	100 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (43547-288-09)
43547-288-10	43547-288	HUMAN PRESCRIPTION DRUG	bupropion hydrochloride SR	Bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20141101	N/A	ANDA	ANDA202304	Solco Healthcare US LLC	BUPROPION HYDROCHLORIDE	100 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (43547-288-10)
43547-288-50	43547-288	HUMAN PRESCRIPTION DRUG	bupropion hydrochloride SR	Bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20141101	N/A	ANDA	ANDA202304	Solco Healthcare US LLC	BUPROPION HYDROCHLORIDE	100 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (43547-288-50)