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
45865-622-90	45865-622	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20071221	N/A	ANDA	ANDA077056	Medsource Pharmaceuticals	PANTOPRAZOLE SODIUM	20 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (45865-622-90)
45865-622-60	45865-622	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20150911	N/A	ANDA	ANDA077056	Medsource Pharmaceuticals	PANTOPRAZOLE SODIUM	20 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (45865-622-60)
45865-622-30	45865-622	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20150911	N/A	ANDA	ANDA077056	Medsource Pharmaceuticals	PANTOPRAZOLE SODIUM	20 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (45865-622-30)
71610-103-09	71610-103	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20180726	N/A	ANDA	ANDA077056	Aphena Pharma Solutions - Tennessee, LLC	PANTOPRAZOLE SODIUM	20 mg/1	9000 TABLET, DELAYED RELEASE in 1 BOTTLE (71610-103-09)
43353-343-30	43353-343	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20170808	N/A	ANDA	ANDA077056	Aphena Pharma Solutions - Tennessee, LLC	PANTOPRAZOLE SODIUM	40 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (43353-343-30)
43353-343-53	43353-343	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20170622	N/A	ANDA	ANDA077056	Aphena Pharma Solutions - Tennessee, LLC	PANTOPRAZOLE SODIUM	40 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (43353-343-53)