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
13107-072-99	13107-072	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	3.75 mg/1; 3.75 mg/1; 3.75 mg/1; 3.75 mg/1	1000 TABLET in 1 BOTTLE (13107-072-99)
13107-074-50	13107-074	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	7.5 mg/1; 7.5 mg/1; 7.5 mg/1; 7.5 mg/1	50 TABLET in 1 BOTTLE (13107-074-50)
13107-074-99	13107-074	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	7.5 mg/1; 7.5 mg/1; 7.5 mg/1; 7.5 mg/1	1000 TABLET in 1 BOTTLE (13107-074-99)