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
47335-737-86	47335-737	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20200301	N/A	ANDA	ANDA078866	Sun Pharmaceutical Industries, Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-737-86)
47335-737-88	47335-737	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20200301	N/A	ANDA	ANDA078866	Sun Pharmaceutical Industries, Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-737-88)
47335-738-08	47335-738	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20200301	N/A	ANDA	ANDA078866	Sun Pharmaceutical Industries, Inc.	BUPROPION HYDROCHLORIDE	200 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-738-08)
47335-738-13	47335-738	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20200301	N/A	ANDA	ANDA078866	Sun Pharmaceutical Industries, Inc.	BUPROPION HYDROCHLORIDE	200 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-738-13)
47335-738-86	47335-738	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20200301	N/A	ANDA	ANDA078866	Sun Pharmaceutical Industries, Inc.	BUPROPION HYDROCHLORIDE	200 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-738-86)
47335-738-88	47335-738	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20200301	N/A	ANDA	ANDA078866	Sun Pharmaceutical Industries, Inc.	BUPROPION HYDROCHLORIDE	200 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-738-88)