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
0615-8261-39	0615-8261	HUMAN PRESCRIPTION DRUG	bupropion Hydrochloride	bupropion Hydrochloride	TABLET	ORAL	20190108	N/A	ANDA	ANDA206975	NCS HealthCare of KY, LLC dba Vangard Labs	BUPROPION HYDROCHLORIDE	75 mg/1	30 TABLET in 1 BLISTER PACK (0615-8261-39)
0615-8296-39	0615-8296	HUMAN PRESCRIPTION DRUG	bupropion Hydrochloride	bupropion Hydrochloride	TABLET	ORAL	20190702	N/A	ANDA	ANDA206975	NCS HealthCare of KY, Inc dba Vangard Labs	BUPROPION HYDROCHLORIDE	100 mg/1	30 TABLET in 1 BLISTER PACK (0615-8296-39)
43063-994-30	43063-994	HUMAN PRESCRIPTION DRUG	bupropion Hydrochloride	bupropion Hydrochloride	TABLET	ORAL	20190620	N/A	ANDA	ANDA206975	PD-Rx Pharmaceuticals, Inc.	BUPROPION HYDROCHLORIDE	100 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (43063-994-30)
23155-192-10	23155-192	HUMAN PRESCRIPTION DRUG	bupropion Hydrochloride	bupropion Hydrochloride	TABLET	ORAL	20160819	N/A	ANDA	ANDA206975	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	BUPROPION HYDROCHLORIDE	100 mg/1	1000 TABLET in 1 BOTTLE (23155-192-10)
51655-390-25	51655-390	HUMAN PRESCRIPTION DRUG	bupropion Hydrochloride	bupropion Hydrochloride	TABLET	ORAL	20220128	N/A	ANDA	ANDA206975	Northwind Pharmaceuticals	BUPROPION HYDROCHLORIDE	100 mg/1	60 TABLET in 1 BOTTLE, PLASTIC (51655-390-25)
51655-390-26	51655-390	HUMAN PRESCRIPTION DRUG	bupropion Hydrochloride	bupropion Hydrochloride	TABLET	ORAL	20220128	N/A	ANDA	ANDA206975	Northwind Pharmaceuticals	BUPROPION HYDROCHLORIDE	100 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (51655-390-26)
70518-2934-0	70518-2934	HUMAN PRESCRIPTION DRUG	bupropion Hydrochloride	bupropion Hydrochloride	TABLET	ORAL	20201104	N/A	ANDA	ANDA206975	REMEDYREPACK INC.	BUPROPION HYDROCHLORIDE	75 mg/1	30 TABLET in 1 BLISTER PACK (70518-2934-0)
62135-723-90	62135-723	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET	ORAL	20230811	N/A	ANDA	ANDA206975	Chartwell RX, LLC	BUPROPION HYDROCHLORIDE	75 mg/1	90 TABLET in 1 BOTTLE (62135-723-90)
62135-724-90	62135-724	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET	ORAL	20230811	N/A	ANDA	ANDA206975	Chartwell RX, LLC	BUPROPION HYDROCHLORIDE	100 mg/1	90 TABLET in 1 BOTTLE (62135-724-90)
23155-192-01	23155-192	HUMAN PRESCRIPTION DRUG	bupropion Hydrochloride	bupropion Hydrochloride	TABLET	ORAL	20160819	N/A	ANDA	ANDA206975	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	BUPROPION HYDROCHLORIDE	100 mg/1	100 TABLET in 1 BOTTLE (23155-192-01)
23155-191-10	23155-191	HUMAN PRESCRIPTION DRUG	bupropion Hydrochloride	bupropion Hydrochloride	TABLET	ORAL	20160819	N/A	ANDA	ANDA206975	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	BUPROPION HYDROCHLORIDE	75 mg/1	1000 TABLET in 1 BOTTLE (23155-191-10)
23155-191-01	23155-191	HUMAN PRESCRIPTION DRUG	bupropion Hydrochloride	bupropion Hydrochloride	TABLET	ORAL	20160819	N/A	ANDA	ANDA206975	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	BUPROPION HYDROCHLORIDE	75 mg/1	100 TABLET in 1 BOTTLE (23155-191-01)