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
65162-636-09	65162-636	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	Pantoprazole	TABLET, DELAYED RELEASE	ORAL	20160620	N/A	ANDA	ANDA205119	Amneal Pharmaceuticals LLC	PANTOPRAZOLE SODIUM	20 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (65162-636-09)
65162-636-03	65162-636	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	Pantoprazole	TABLET, DELAYED RELEASE	ORAL	20160620	N/A	ANDA	ANDA205119	Amneal Pharmaceuticals LLC	PANTOPRAZOLE SODIUM	20 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (65162-636-03)
63187-974-30	63187-974	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	Pantoprazole	TABLET, DELAYED RELEASE	ORAL	20160620	N/A	ANDA	ANDA205119	Proficient Rx LP	PANTOPRAZOLE SODIUM	40 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-974-30)
63187-974-60	63187-974	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	Pantoprazole	TABLET, DELAYED RELEASE	ORAL	20160620	N/A	ANDA	ANDA205119	Proficient Rx LP	PANTOPRAZOLE SODIUM	40 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-974-60)
63187-974-90	63187-974	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	Pantoprazole	TABLET, DELAYED RELEASE	ORAL	20160620	N/A	ANDA	ANDA205119	Proficient Rx LP	PANTOPRAZOLE SODIUM	40 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-974-90)
80425-0085-3	80425-0085	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium DR	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20160620	N/A	ANDA	ANDA205119	Advanced Rx of Tennessee, LLC	PANTOPRAZOLE SODIUM	20 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0085-3)