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
71335-0791-4	71335-0791	HUMAN PRESCRIPTION DRUG	bupropion Hydrochloride	bupropion Hydrochloride	TABLET	ORAL	20190619	N/A	ANDA	ANDA206975	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	75 mg/1	7 TABLET in 1 BOTTLE (71335-0791-4)
71335-0791-1	71335-0791	HUMAN PRESCRIPTION DRUG	bupropion Hydrochloride	bupropion Hydrochloride	TABLET	ORAL	20180426	N/A	ANDA	ANDA206975	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	75 mg/1	30 TABLET in 1 BOTTLE (71335-0791-1)
71335-0791-2	71335-0791	HUMAN PRESCRIPTION DRUG	bupropion Hydrochloride	bupropion Hydrochloride	TABLET	ORAL	20190619	N/A	ANDA	ANDA206975	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	75 mg/1	60 TABLET in 1 BOTTLE (71335-0791-2)
72789-544-90	72789-544	HUMAN PRESCRIPTION DRUG	bupropion Hydrochloride	bupropion Hydrochloride	TABLET	ORAL	20260105	N/A	ANDA	ANDA206975	PD-Rx Pharmaceuticals, Inc.	BUPROPION HYDROCHLORIDE	100 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (72789-544-90)
51655-390-25	51655-390	HUMAN PRESCRIPTION DRUG	bupropion Hydrochloride	bupropion Hydrochloride	TABLET	ORAL	20220128	N/A	ANDA	ANDA206975	Northwind Health Company, LLC	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 Health Company, LLC	BUPROPION HYDROCHLORIDE	100 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (51655-390-26)
67046-1587-3	67046-1587	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET	ORAL	20250916	N/A	ANDA	ANDA206975	Coupler LLC	BUPROPION HYDROCHLORIDE	75 mg/1	30 TABLET in 1 BLISTER PACK (67046-1587-3)
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)
67046-1562-3	67046-1562	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET	ORAL	20250521	N/A	ANDA	ANDA206975	Coupler LLC	BUPROPION HYDROCHLORIDE	100 mg/1	30 TABLET in 1 BLISTER PACK (67046-1562-3)
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)
67046-1672-3	67046-1672	HUMAN PRESCRIPTION DRUG	bupropion Hydrochloride	bupropion Hydrochloride	TABLET	ORAL	20260427	N/A	ANDA	ANDA206975	Coupler LLC	BUPROPION HYDROCHLORIDE	100 mg/1	30 TABLET in 1 BLISTER PACK (67046-1672-3)
0904-7530-60	0904-7530	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET	ORAL	20250130	N/A	ANDA	ANDA206975	MAJOR PHARMACEUTICALS	BUPROPION HYDROCHLORIDE	100 mg/1	100 TABLET in 1 BOTTLE (0904-7530-60)
0904-7529-60	0904-7529	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET	ORAL	20250130	N/A	ANDA	ANDA206975	MAJOR PHARMACEUTICALS	BUPROPION HYDROCHLORIDE	75 mg/1	100 TABLET in 1 BOTTLE (0904-7529-60)