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
43598-863-10	43598-863	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE (SR)	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20160817	N/A	ANDA	ANDA206122	Dr. Reddy's Laboratories Inc	BUPROPION HYDROCHLORIDE	150 mg/1	1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (43598-863-10)
43598-863-30	43598-863	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE (SR)	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20160817	N/A	ANDA	ANDA206122	Dr. Reddy's Laboratories Inc	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (43598-863-30)
43598-863-60	43598-863	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE (SR)	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20160817	N/A	ANDA	ANDA206122	Dr. Reddy's Laboratories Inc	BUPROPION HYDROCHLORIDE	150 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (43598-863-60)
50090-5101-0	50090-5101	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE (SR)	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20200713	N/A	ANDA	ANDA206122	A-S Medication Solutions	BUPROPION HYDROCHLORIDE	150 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-5101-0)
50090-5101-1	50090-5101	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE (SR)	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20200713	N/A	ANDA	ANDA206122	A-S Medication Solutions	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-5101-1)
50228-338-11	50228-338	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (SR)	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190501	N/A	ANDA	ANDA206122	ScieGen Pharmaceuticals, Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50228-338-11)
50228-338-31	50228-338	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (SR)	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190501	N/A	ANDA	ANDA206122	ScieGen Pharmaceuticals, Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50228-338-31)
50228-338-61	50228-338	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (SR)	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190501	N/A	ANDA	ANDA206122	ScieGen Pharmaceuticals, Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50228-338-61)