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
72162-1087-1	72162-1087	HUMAN PRESCRIPTION DRUG	AMPHETAMINE SULFATE	amphetamine sulfate	TABLET	ORAL	20240405	N/A	ANDA	ANDA212901	Bryant Ranch Prepack	AMPHETAMINE SULFATE	5 mg/1	100 TABLET in 1 BOTTLE (72162-1087-1)
72162-1088-1	72162-1088	HUMAN PRESCRIPTION DRUG	AMPHETAMINE SULFATE	amphetamine sulfate	TABLET	ORAL	20240405	N/A	ANDA	ANDA212901	Bryant Ranch Prepack	AMPHETAMINE SULFATE	10 mg/1	100 TABLET in 1 BOTTLE (72162-1088-1)
63629-2078-1	63629-2078	HUMAN PRESCRIPTION DRUG	AMPHETAMINE SULFATE	amphetamine sulfate	TABLET	ORAL	20211221	N/A	ANDA	ANDA212901	Bryant Ranch Prepack	AMPHETAMINE SULFATE	10 mg/1	100 TABLET in 1 BOTTLE (63629-2078-1)
63629-2079-1	63629-2079	HUMAN PRESCRIPTION DRUG	AMPHETAMINE SULFATE	amphetamine sulfate	TABLET	ORAL	20240402	N/A	ANDA	ANDA212901	Bryant Ranch Prepack	AMPHETAMINE SULFATE	5 mg/1	100 TABLET in 1 BOTTLE (63629-2079-1)
0527-2524-37	0527-2524	HUMAN PRESCRIPTION DRUG	AMPHETAMINE SULFATE	amphetamine sulfate	TABLET	ORAL	20200601	N/A	ANDA	ANDA212901	Lannett Company, Inc.	AMPHETAMINE SULFATE	5 mg/1	100 TABLET in 1 BOTTLE (0527-2524-37)
0527-2525-37	0527-2525	HUMAN PRESCRIPTION DRUG	AMPHETAMINE SULFATE	amphetamine sulfate	TABLET	ORAL	20200601	N/A	ANDA	ANDA212901	Lannett Company, Inc.	AMPHETAMINE SULFATE	10 mg/1	100 TABLET in 1 BOTTLE (0527-2525-37)
71335-2990-1	71335-2990	HUMAN PRESCRIPTION DRUG	AMPHETAMINE SULFATE	amphetamine sulfate	TABLET	ORAL	20260204	N/A	ANDA	ANDA212901	Bryant Ranch Prepack	AMPHETAMINE SULFATE	10 mg/1	120 TABLET in 1 BOTTLE (71335-2990-1)