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
71335-1984-4	71335-1984	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20240718	N/A	ANDA	ANDA205794	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	200 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71335-1984-4)
71335-1984-5	71335-1984	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20240718	N/A	ANDA	ANDA205794	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	200 mg/1	120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71335-1984-5)
71335-1984-6	71335-1984	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20240718	N/A	ANDA	ANDA205794	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	200 mg/1	28 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71335-1984-6)
50228-175-01	50228-175	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20180420	N/A	ANDA	ANDA205794	ScieGen Pharmaceuticals, Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50228-175-01)
50228-175-05	50228-175	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20180420	N/A	ANDA	ANDA205794	ScieGen Pharmaceuticals, Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50228-175-05)
50228-175-10	50228-175	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20180420	N/A	ANDA	ANDA205794	ScieGen Pharmaceuticals, Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50228-175-10)
50228-175-30	50228-175	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20180420	N/A	ANDA	ANDA205794	ScieGen Pharmaceuticals, Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50228-175-30)
77771-175-05	77771-175	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20210415	N/A	ANDA	ANDA205794	Radha Pharmaceuticals, Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (77771-175-05)
77771-175-60	77771-175	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20210415	N/A	ANDA	ANDA205794	Radha Pharmaceuticals, Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (77771-175-60)
50228-174-01	50228-174	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20180420	N/A	ANDA	ANDA205794	ScieGen Pharmaceuticals, Inc.	BUPROPION HYDROCHLORIDE	100 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50228-174-01)
50228-174-05	50228-174	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20180420	N/A	ANDA	ANDA205794	ScieGen Pharmaceuticals, Inc.	BUPROPION HYDROCHLORIDE	100 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50228-174-05)
50228-174-10	50228-174	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20180420	N/A	ANDA	ANDA205794	ScieGen Pharmaceuticals, Inc.	BUPROPION HYDROCHLORIDE	100 mg/1	1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50228-174-10)
50228-174-30	50228-174	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20180420	N/A	ANDA	ANDA205794	ScieGen Pharmaceuticals, Inc.	BUPROPION HYDROCHLORIDE	100 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50228-174-30)
50228-174-60	50228-174	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20180420	N/A	ANDA	ANDA205794	ScieGen Pharmaceuticals, Inc.	BUPROPION HYDROCHLORIDE	100 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50228-174-60)
50228-175-60	50228-175	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20180420	N/A	ANDA	ANDA205794	ScieGen Pharmaceuticals, Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50228-175-60)
70518-4056-1	70518-4056	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20250123	N/A	ANDA	ANDA205794	REMEDYREPACK INC.	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-4056-1)
68788-7819-3	68788-7819	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20201113	N/A	ANDA	ANDA205794	Preferred Pharmaceuticals, Inc.	BUPROPION HYDROCHLORIDE	100 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-7819-3)
68788-7819-6	68788-7819	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20201113	N/A	ANDA	ANDA205794	Preferred Pharmaceuticals, Inc.	BUPROPION HYDROCHLORIDE	100 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-7819-6)
68788-7819-9	68788-7819	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20201113	N/A	ANDA	ANDA205794	Preferred Pharmaceuticals, Inc.	BUPROPION HYDROCHLORIDE	100 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-7819-9)