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
72189-349-30	72189-349	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE SR	BUPROPION HYDROCHLORIDE SR	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20220809	N/A	ANDA	ANDA205794	DirectRx	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72189-349-30)
72189-349-60	72189-349	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE SR	BUPROPION HYDROCHLORIDE SR	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20220422	N/A	ANDA	ANDA205794	DirectRx	BUPROPION HYDROCHLORIDE	150 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72189-349-60)
50090-6871-0	50090-6871	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20231204	N/A	ANDA	ANDA205794	A-S Medication Solutions	BUPROPION HYDROCHLORIDE	150 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-6871-0)
50090-6871-1	50090-6871	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20231204	N/A	ANDA	ANDA205794	A-S Medication Solutions	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-6871-1)
50090-6871-2	50090-6871	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20231204	N/A	ANDA	ANDA205794	A-S Medication Solutions	BUPROPION HYDROCHLORIDE	150 mg/1	180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-6871-2)
50090-6871-3	50090-6871	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20231204	N/A	ANDA	ANDA205794	A-S Medication Solutions	BUPROPION HYDROCHLORIDE	150 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-6871-3)
50090-6872-0	50090-6872	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20231204	N/A	ANDA	ANDA205794	A-S Medication Solutions	BUPROPION HYDROCHLORIDE	150 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-6872-0)
71335-1702-4	71335-1702	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20240404	N/A	ANDA	ANDA205794	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	150 mg/1	120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1702-4)
71335-1702-5	71335-1702	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20240404	N/A	ANDA	ANDA205794	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	150 mg/1	45 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1702-5)
71335-1702-6	71335-1702	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20200908	N/A	ANDA	ANDA205794	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	150 mg/1	180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1702-6)
71335-1702-7	71335-1702	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20240404	N/A	ANDA	ANDA205794	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	150 mg/1	28 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1702-7)
71335-1702-8	71335-1702	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20240404	N/A	ANDA	ANDA205794	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	150 mg/1	56 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1702-8)
71335-1702-9	71335-1702	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20240404	N/A	ANDA	ANDA205794	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	150 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1702-9)
50090-7130-0	50090-7130	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20240415	N/A	ANDA	ANDA205794	A-S Medication Solutions	BUPROPION HYDROCHLORIDE	100 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7130-0)
71335-1702-3	71335-1702	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20201006	N/A	ANDA	ANDA205794	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1702-3)
71335-1702-2	71335-1702	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20201120	N/A	ANDA	ANDA205794	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	150 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1702-2)
71335-1702-1	71335-1702	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20200916	N/A	ANDA	ANDA205794	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	150 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1702-1)
71335-1866-1	71335-1866	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20210621	N/A	ANDA	ANDA205794	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	100 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71335-1866-1)
71335-1866-5	71335-1866	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20240717	N/A	ANDA	ANDA205794	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	100 mg/1	28 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71335-1866-5)
71335-1866-6	71335-1866	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20220906	N/A	ANDA	ANDA205794	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	100 mg/1	120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71335-1866-6)