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
72162-2054-3	72162-2054	HUMAN PRESCRIPTION DRUG	Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate	Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate	TABLET	ORAL	20230614	N/A	ANDA	ANDA211352	Bryant Ranch Prepack	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	30 TABLET in 1 BOTTLE (72162-2054-3)
72162-2054-6	72162-2054	HUMAN PRESCRIPTION DRUG	Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate	Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate	TABLET	ORAL	20230614	N/A	ANDA	ANDA211352	Bryant Ranch Prepack	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	60 TABLET in 1 BOTTLE (72162-2054-6)
72162-2054-9	72162-2054	HUMAN PRESCRIPTION DRUG	Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate	Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate	TABLET	ORAL	20230614	N/A	ANDA	ANDA211352	Bryant Ranch Prepack	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	90 TABLET in 1 BOTTLE (72162-2054-9)