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
72789-070-90	72789-070	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20240607	N/A	ANDA	ANDA076143	PD-Rx Pharmaceuticals, Inc.	BUPROPION HYDROCHLORIDE	100 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-070-90)
50090-1869-0	50090-1869	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20150610	N/A	ANDA	ANDA076143	A-S Medication Solutions	BUPROPION HYDROCHLORIDE	100 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (50090-1869-0)
50090-1869-3	50090-1869	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20150610	N/A	ANDA	ANDA076143	A-S Medication Solutions	BUPROPION HYDROCHLORIDE	100 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (50090-1869-3)
71335-0013-1	71335-0013	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20180308	N/A	ANDA	ANDA076143	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	75 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-0013-1)
71335-0013-2	71335-0013	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20180221	N/A	ANDA	ANDA076143	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	75 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-0013-2)
71335-0013-3	71335-0013	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20240709	N/A	ANDA	ANDA076143	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	75 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-0013-3)
71335-0013-4	71335-0013	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20240709	N/A	ANDA	ANDA076143	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	75 mg/1	7 TABLET, FILM COATED in 1 BOTTLE (71335-0013-4)
71335-0013-5	71335-0013	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20240709	N/A	ANDA	ANDA076143	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	75 mg/1	14 TABLET, FILM COATED in 1 BOTTLE (71335-0013-5)
71335-0013-6	71335-0013	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20240709	N/A	ANDA	ANDA076143	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	75 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (71335-0013-6)
71335-0013-7	71335-0013	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20240709	N/A	ANDA	ANDA076143	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	75 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (71335-0013-7)
72789-070-30	72789-070	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20200326	N/A	ANDA	ANDA076143	PD-Rx Pharmaceuticals, Inc.	BUPROPION HYDROCHLORIDE	100 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-070-30)
72162-2098-1	72162-2098	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20060117	N/A	ANDA	ANDA076143	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	75 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (72162-2098-1)
72162-2097-1	72162-2097	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20060117	N/A	ANDA	ANDA076143	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	100 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (72162-2097-1)
71335-0182-3	71335-0182	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20240709	N/A	ANDA	ANDA076143	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	100 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (71335-0182-3)
71335-0182-5	71335-0182	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20240709	N/A	ANDA	ANDA076143	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	100 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (71335-0182-5)
71335-0182-6	71335-0182	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20240709	N/A	ANDA	ANDA076143	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	100 mg/1	15 TABLET, FILM COATED in 1 BOTTLE (71335-0182-6)
71335-0182-7	71335-0182	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20210428	N/A	ANDA	ANDA076143	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	100 mg/1	21 TABLET, FILM COATED in 1 BOTTLE (71335-0182-7)
50268-142-15	50268-142	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20170802	N/A	ANDA	ANDA076143	AvPAK	BUPROPION HYDROCHLORIDE	75 mg/1	50 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-142-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-142-11)
50268-143-15	50268-143	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20170802	N/A	ANDA	ANDA076143	AvPAK	BUPROPION HYDROCHLORIDE	100 mg/1	50 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-143-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-143-11)
71335-0182-4	71335-0182	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20180328	N/A	ANDA	ANDA076143	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	100 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-0182-4)