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
0187-0731-07	0187-0731	HUMAN PRESCRIPTION DRUG	WELLBUTRIN XL	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20030829	N/A	NDA	NDA021515	Bausch Health US LLC	BUPROPION HYDROCHLORIDE	300 mg/1	7 TABLET, EXTENDED RELEASE in 1 BOTTLE (0187-0731-07)
0187-0731-30	0187-0731	HUMAN PRESCRIPTION DRUG	WELLBUTRIN XL	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20030829	N/A	NDA	NDA021515	Bausch Health US LLC	BUPROPION HYDROCHLORIDE	300 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (0187-0731-30)
0187-0730-90	0187-0730	HUMAN PRESCRIPTION DRUG	WELLBUTRIN XL	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20030829	N/A	NDA	NDA021515	Bausch Health US LLC	BUPROPION HYDROCHLORIDE	150 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (0187-0730-90)
0187-0730-30	0187-0730	HUMAN PRESCRIPTION DRUG	WELLBUTRIN XL	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20030829	N/A	NDA	NDA021515	Bausch Health US LLC	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (0187-0730-30)
0187-0730-07	0187-0730	HUMAN PRESCRIPTION DRUG	WELLBUTRIN XL	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20030829	N/A	NDA	NDA021515	Bausch Health US LLC	BUPROPION HYDROCHLORIDE	150 mg/1	7 TABLET, EXTENDED RELEASE in 1 BOTTLE (0187-0730-07)