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
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)
77771-176-60	77771-176	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20210415	N/A	ANDA	ANDA205794	Radha Pharmaceuticals, Inc.	BUPROPION HYDROCHLORIDE	200 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (77771-176-60)
63629-8473-1	63629-8473	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20180420	N/A	ANDA	ANDA205794	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	150 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (63629-8473-1)
72189-349-60	72189-349	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE SR	BUPROPION HYDROCHLORIDE SR	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20220422	N/A	ANDA	ANDA205794	DirectRx	BUPROPION HYDROCHLORIDE	150 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72189-349-60)
77771-174-60	77771-174	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20210415	N/A	ANDA	ANDA205794	Radha Pharmaceuticals, Inc.	BUPROPION HYDROCHLORIDE	100 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (77771-174-60)
77771-174-05	77771-174	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20210415	N/A	ANDA	ANDA205794	Radha Pharmaceuticals, Inc.	BUPROPION HYDROCHLORIDE	100 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (77771-174-05)
72189-349-30	72189-349	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE SR	BUPROPION HYDROCHLORIDE SR	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20220809	N/A	ANDA	ANDA205794	DirectRx	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72189-349-30)
82868-019-96	82868-019	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20240219	N/A	ANDA	ANDA205794	Northwind Health Company, LLC	BUPROPION HYDROCHLORIDE	150 mg/1	180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82868-019-96)
82868-019-30	82868-019	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20240314	N/A	ANDA	ANDA205794	Northwind Health Company, LLC	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82868-019-30)
82868-019-60	82868-019	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20231019	N/A	ANDA	ANDA205794	Northwind Health Company, LLC	BUPROPION HYDROCHLORIDE	150 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82868-019-60)
82868-019-90	82868-019	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20250102	N/A	ANDA	ANDA205794	Northwind Health Company, LLC	BUPROPION HYDROCHLORIDE	150 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82868-019-90)
71335-1702-1	71335-1702	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20200916	N/A	ANDA	ANDA205794	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	150 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1702-1)
71335-1702-5	71335-1702	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20240404	N/A	ANDA	ANDA205794	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	150 mg/1	45 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1702-5)
71335-1702-6	71335-1702	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20200908	N/A	ANDA	ANDA205794	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	150 mg/1	180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1702-6)
71335-1702-7	71335-1702	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20240404	N/A	ANDA	ANDA205794	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	150 mg/1	28 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1702-7)
71335-1702-8	71335-1702	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20240404	N/A	ANDA	ANDA205794	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	150 mg/1	56 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1702-8)
71335-1702-9	71335-1702	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20240404	N/A	ANDA	ANDA205794	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	150 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1702-9)
71335-1702-2	71335-1702	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20201120	N/A	ANDA	ANDA205794	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	150 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1702-2)
71335-1702-3	71335-1702	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20201006	N/A	ANDA	ANDA205794	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1702-3)