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
50090-7322-0	50090-7322	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20241015	N/A	ANDA	ANDA216766	A-S Medication Solutions	BUPROPION HYDROCHLORIDE	150 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7322-0)
50090-7322-1	50090-7322	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20241015	N/A	ANDA	ANDA216766	A-S Medication Solutions	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7322-1)
42806-413-60	42806-413	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20230228	N/A	ANDA	ANDA216766	Epic Pharma, LLC	BUPROPION HYDROCHLORIDE	150 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42806-413-60)