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
70436-058-01	70436-058	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20201102	N/A	ANDA	ANDA211347	Slate Run Pharmaceuticals, LLC	BUPROPION HYDROCHLORIDE	100 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-058-01)
70436-058-02	70436-058	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20201102	N/A	ANDA	ANDA211347	Slate Run Pharmaceuticals, LLC	BUPROPION HYDROCHLORIDE	100 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-058-02)
70436-058-05	70436-058	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20201102	N/A	ANDA	ANDA211347	Slate Run Pharmaceuticals, LLC	BUPROPION HYDROCHLORIDE	100 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-058-05)
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)
70436-060-01	70436-060	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20201102	N/A	ANDA	ANDA211347	Slate Run Pharmaceuticals, LLC	BUPROPION HYDROCHLORIDE	200 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-060-01)
70436-060-02	70436-060	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20201102	N/A	ANDA	ANDA211347	Slate Run Pharmaceuticals, LLC	BUPROPION HYDROCHLORIDE	200 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-060-02)
70436-060-05	70436-060	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20201102	N/A	ANDA	ANDA211347	Slate Run Pharmaceuticals, LLC	BUPROPION HYDROCHLORIDE	200 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-060-05)
70518-3811-0	70518-3811	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20230730	N/A	ANDA	ANDA211347	REMEDYREPACK INC.	BUPROPION HYDROCHLORIDE	200 mg/1	30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-3811-0)
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	20220706	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	20220706	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	20220706	N/A	ANDA	ANDA211347	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	150 mg/1	28 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1837-7)
71335-1837-8	71335-1837	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20220706	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	20220706	N/A	ANDA	ANDA211347	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	150 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1837-9)