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
24979-101-06	24979-101	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20180830	20260630	ANDA	ANDA210081	Upsher-Smith Laboratories, LLC	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (24979-101-06)
24979-101-07	24979-101	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20180830	20260630	ANDA	ANDA210081	Upsher-Smith Laboratories, LLC	BUPROPION HYDROCHLORIDE	150 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (24979-101-07)
24979-102-02	24979-102	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20180830	20260630	ANDA	ANDA210081	Upsher-Smith Laboratories, LLC	BUPROPION HYDROCHLORIDE	300 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (24979-102-02)
50090-7109-0	50090-7109	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240311	N/A	ANDA	ANDA210081	A-S Medication Solutions	BUPROPION HYDROCHLORIDE	150 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50090-7109-0)
50090-7110-0	50090-7110	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240311	N/A	ANDA	ANDA210081	A-S Medication Solutions	BUPROPION HYDROCHLORIDE	150 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7110-0)
50090-7110-1	50090-7110	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240311	N/A	ANDA	ANDA210081	A-S Medication Solutions	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7110-1)
50090-7110-2	50090-7110	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240311	N/A	ANDA	ANDA210081	A-S Medication Solutions	BUPROPION HYDROCHLORIDE	150 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7110-2)