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
0615-8526-39	0615-8526	HUMAN PRESCRIPTION DRUG	bupropion	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240910	20260131	ANDA	ANDA202304	NCS HealthCare of KY, LLC dba Vangard Labs	BUPROPION HYDROCHLORIDE	100 mg/1	30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0615-8526-39)
0615-8262-39	0615-8262	HUMAN PRESCRIPTION DRUG	bupropion	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20190108	20260228	ANDA	ANDA202304	NCS HealthCare of KY, LLC dba Vangard Labs	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0615-8262-39)
71205-565-60	71205-565	HUMAN PRESCRIPTION DRUG	bupropion	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20210511	N/A	ANDA	ANDA202304	Proficient Rx LP	BUPROPION HYDROCHLORIDE	150 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-565-60)
71205-565-30	71205-565	HUMAN PRESCRIPTION DRUG	bupropion	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20210511	N/A	ANDA	ANDA202304	Proficient Rx LP	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-565-30)
71205-565-90	71205-565	HUMAN PRESCRIPTION DRUG	bupropion	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20210511	N/A	ANDA	ANDA202304	Proficient Rx LP	BUPROPION HYDROCHLORIDE	150 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-565-90)
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
55154-0183-0	55154-0183	HUMAN PRESCRIPTION DRUG	bupropion hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20250609	N/A	ANDA	ANDA202304	Cardinal Health 107, LLC	BUPROPION HYDROCHLORIDE	150 mg/1	10 BLISTER PACK in 1 BAG (55154-0183-0) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
51655-357-26	51655-357	HUMAN PRESCRIPTION DRUG	bupropion	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20200528	N/A	ANDA	ANDA202304	Northwind Pharmaceuticals, LLC	BUPROPION HYDROCHLORIDE	150 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-357-26)
51655-357-52	51655-357	HUMAN PRESCRIPTION DRUG	bupropion	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20220901	N/A	ANDA	ANDA202304	Northwind Pharmaceuticals, LLC	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-357-52)
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)
43547-288-10	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)
43547-289-09	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)
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)
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)