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
13107-070-05	13107-070	HUMAN PRESCRIPTION DRUG	Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate	Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate	TABLET	ORAL	20131127	N/A	ANDA	ANDA202424	Aurolife Pharma, LLC	AMPHETAMINE ASPARTATE MONOHYDRATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE	2.5 mg/1; 2.5 mg/1; 2.5 mg/1; 2.5 mg/1	500 TABLET in 1 BOTTLE (13107-070-05)
16714-952-01	16714-952	HUMAN PRESCRIPTION DRUG	Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate	Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate	TABLET	ORAL	20190320	N/A	ANDA	ANDA202424	NorthStar RxLLC	AMPHETAMINE ASPARTATE MONOHYDRATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE	3.75 mg/1; 3.75 mg/1; 3.75 mg/1; 3.75 mg/1	100 TABLET in 1 BOTTLE (16714-952-01)
16714-953-01	16714-953	HUMAN PRESCRIPTION DRUG	Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate	Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate	TABLET	ORAL	20190320	N/A	ANDA	ANDA202424	NorthStar RxLLC	AMPHETAMINE ASPARTATE MONOHYDRATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE	5 mg/1; 5 mg/1; 5 mg/1; 5 mg/1	100 TABLET in 1 BOTTLE (16714-953-01)