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
71335-1837-1	71335-1837	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20210505	N/A	ANDA	ANDA211347	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	150 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1837-1)
71335-1837-2	71335-1837	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20220217	N/A	ANDA	ANDA211347	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	150 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1837-2)
71335-1837-3	71335-1837	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20210426	N/A	ANDA	ANDA211347	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1837-3)
71335-1837-4	71335-1837	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240717	N/A	ANDA	ANDA211347	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	150 mg/1	120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1837-4)
71335-1837-5	71335-1837	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240717	N/A	ANDA	ANDA211347	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	150 mg/1	45 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1837-5)
71335-1837-6	71335-1837	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20220202	N/A	ANDA	ANDA211347	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	150 mg/1	180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1837-6)
71335-1837-7	71335-1837	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240717	N/A	ANDA	ANDA211347	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	150 mg/1	28 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1837-7)
51655-115-25	51655-115	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20221005	N/A	ANDA	ANDA211347	Northwind Health Company, LLC	BUPROPION HYDROCHLORIDE	150 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-115-25)
51655-115-26	51655-115	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20221115	N/A	ANDA	ANDA211347	Northwind Health Company, LLC	BUPROPION HYDROCHLORIDE	150 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-115-26)
51655-115-52	51655-115	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20221130	N/A	ANDA	ANDA211347	Northwind Health Company, LLC	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-115-52)
51655-115-83	51655-115	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20230105	N/A	ANDA	ANDA211347	Northwind Health Company, LLC	BUPROPION HYDROCHLORIDE	150 mg/1	180 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-115-83)
70436-059-01	70436-059	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20201102	N/A	ANDA	ANDA211347	Slate Run Pharmaceuticals, LLC	BUPROPION HYDROCHLORIDE	150 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-059-01)
70436-059-02	70436-059	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20201102	N/A	ANDA	ANDA211347	Slate Run Pharmaceuticals, LLC	BUPROPION HYDROCHLORIDE	150 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-059-02)
70436-059-05	70436-059	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20201102	N/A	ANDA	ANDA211347	Slate Run Pharmaceuticals, LLC	BUPROPION HYDROCHLORIDE	150 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-059-05)
70436-059-22	70436-059	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20201102	N/A	ANDA	ANDA211347	Slate Run Pharmaceuticals, LLC	BUPROPION HYDROCHLORIDE	150 mg/1	250 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-059-22)
71335-1837-8	71335-1837	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240717	N/A	ANDA	ANDA211347	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	150 mg/1	56 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1837-8)
71335-1837-9	71335-1837	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240717	N/A	ANDA	ANDA211347	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	150 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1837-9)
42806-425-01	42806-425	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20230918	N/A	ANDA	ANDA211347	Epic Pharma, LLC	BUPROPION HYDROCHLORIDE	150 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (42806-425-01)
42806-425-05	42806-425	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20230918	N/A	ANDA	ANDA211347	Epic Pharma, LLC	BUPROPION HYDROCHLORIDE	150 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (42806-425-05)
42806-425-52	42806-425	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20230918	N/A	ANDA	ANDA211347	Epic Pharma, LLC	BUPROPION HYDROCHLORIDE	150 mg/1	250 TABLET, EXTENDED RELEASE in 1 BOTTLE (42806-425-52)