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
71335-1870-2	71335-1870	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240718	N/A	ANDA	ANDA211347	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	200 mg/1	180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1870-2)
71335-1870-3	71335-1870	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240718	N/A	ANDA	ANDA211347	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	200 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1870-3)
71335-1870-4	71335-1870	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240718	N/A	ANDA	ANDA211347	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	200 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1870-4)
71335-1870-5	71335-1870	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240718	N/A	ANDA	ANDA211347	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	200 mg/1	120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1870-5)
71335-1870-6	71335-1870	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240718	N/A	ANDA	ANDA211347	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	200 mg/1	28 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1870-6)