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
63629-2498-1	63629-2498	HUMAN PRESCRIPTION DRUG	Amphetamine Sulfate	Amphetamine Sulfate	TABLET	ORAL	20180329	N/A	ANDA	ANDA200166	Bryant Ranch Prepack	AMPHETAMINE SULFATE	10 mg/1	100 TABLET in 1 BOTTLE (63629-2498-1)
63629-2499-1	63629-2499	HUMAN PRESCRIPTION DRUG	Amphetamine Sulfate	Amphetamine Sulfate	TABLET	ORAL	20180329	N/A	ANDA	ANDA200166	Bryant Ranch Prepack	AMPHETAMINE SULFATE	5 mg/1	100 TABLET in 1 BOTTLE (63629-2499-1)
52536-059-03	52536-059	HUMAN PRESCRIPTION DRUG	Amphetamine Sulfate	Amphetamine Sulfate	TABLET	ORAL	20210107	N/A	ANDA	ANDA200166	Wilshire Pharmaceuticals	AMPHETAMINE SULFATE	10 mg/1	30 TABLET in 1 BOTTLE (52536-059-03)
24338-026-03	24338-026	HUMAN PRESCRIPTION DRUG	Evekeo	Amphetamine Sulfate	TABLET	ORAL	20210312	N/A	ANDA	ANDA200166	AZURITY PHARMACEUTICALS, INC.	AMPHETAMINE SULFATE	10 mg/1	30 TABLET in 1 BOTTLE (24338-026-03)
24338-022-03	24338-022	HUMAN PRESCRIPTION DRUG	Evekeo	Amphetamine Sulfate	TABLET	ORAL	20210312	N/A	ANDA	ANDA200166	AZURITY PHARMACEUTICALS, INC.	AMPHETAMINE SULFATE	5 mg/1	30 TABLET in 1 BOTTLE (24338-022-03)
52536-057-03	52536-057	HUMAN PRESCRIPTION DRUG	Amphetamine Sulfate	Amphetamine Sulfate	TABLET	ORAL	20210107	N/A	ANDA	ANDA200166	Wilshire Pharmaceuticals	AMPHETAMINE SULFATE	5 mg/1	30 TABLET in 1 BOTTLE (52536-057-03)