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
0187-5811-07	0187-5811	HUMAN PRESCRIPTION DRUG	Aplenzin	bupropion hydrobromide	TABLET, EXTENDED RELEASE	ORAL	20080423	N/A	NDA	NDA022108	Bausch Health US, LLC	BUPROPION HYDROBROMIDE	348 mg/1	7 TABLET, EXTENDED RELEASE in 1 BOTTLE (0187-5811-07)
0187-5811-30	0187-5811	HUMAN PRESCRIPTION DRUG	Aplenzin	bupropion hydrobromide	TABLET, EXTENDED RELEASE	ORAL	20080423	N/A	NDA	NDA022108	Bausch Health US, LLC	BUPROPION HYDROBROMIDE	348 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (0187-5811-30)
0187-5810-07	0187-5810	HUMAN PRESCRIPTION DRUG	Aplenzin	bupropion hydrobromide	TABLET, EXTENDED RELEASE	ORAL	20080423	N/A	NDA	NDA022108	Bausch Health US, LLC	BUPROPION HYDROBROMIDE	174 mg/1	7 TABLET, EXTENDED RELEASE in 1 BOTTLE (0187-5810-07)
0187-5810-30	0187-5810	HUMAN PRESCRIPTION DRUG	Aplenzin	bupropion hydrobromide	TABLET, EXTENDED RELEASE	ORAL	20080423	N/A	NDA	NDA022108	Bausch Health US, LLC	BUPROPION HYDROBROMIDE	174 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (0187-5810-30)
0187-5812-07	0187-5812	HUMAN PRESCRIPTION DRUG	Aplenzin	bupropion hydrobromide	TABLET, EXTENDED RELEASE	ORAL	20080423	N/A	NDA	NDA022108	Bausch Health US, LLC	BUPROPION HYDROBROMIDE	522 mg/1	7 TABLET, EXTENDED RELEASE in 1 BOTTLE (0187-5812-07)
0187-5812-30	0187-5812	HUMAN PRESCRIPTION DRUG	Aplenzin	bupropion hydrobromide	TABLET, EXTENDED RELEASE	ORAL	20080423	N/A	NDA	NDA022108	Bausch Health US, LLC	BUPROPION HYDROBROMIDE	522 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (0187-5812-30)