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
71335-0801-5	71335-0801	HUMAN PRESCRIPTION DRUG	bupropion	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240809	N/A	ANDA	ANDA202304	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	200 mg/1	120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0801-5)
71335-0801-6	71335-0801	HUMAN PRESCRIPTION DRUG	bupropion	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240809	N/A	ANDA	ANDA202304	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	200 mg/1	28 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0801-6)
43547-289-06	43547-289	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	150 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (43547-289-06)
43547-289-09	43547-289	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	150 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (43547-289-09)
43547-289-10	43547-289	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	150 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (43547-289-10)
43547-289-25	43547-289	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	150 mg/1	250 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (43547-289-25)
43547-289-50	43547-289	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	150 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (43547-289-50)
51655-357-26	51655-357	HUMAN PRESCRIPTION DRUG	bupropion	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20200528	N/A	ANDA	ANDA202304	Northwind Health Company, LLC	BUPROPION HYDROCHLORIDE	150 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-357-26)
51655-357-52	51655-357	HUMAN PRESCRIPTION DRUG	bupropion	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20220901	N/A	ANDA	ANDA202304	Northwind Health Company, LLC	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-357-52)
0904-7099-61	0904-7099	HUMAN PRESCRIPTION DRUG	bupropion hydrochloride SR	Bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20260121	N/A	ANDA	ANDA202304	Major Pharmaceuticals	BUPROPION HYDROCHLORIDE	100 mg/1	100 BLISTER PACK in 1 CARTON (0904-7099-61) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK