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
80425-0179-2	80425-0179	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium DR	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20110119	N/A	ANDA	ANDA090970	Advanced Rx Pharmacy of Tennessee, LLC	PANTOPRAZOLE SODIUM	20 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0179-2)
80425-0179-3	80425-0179	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium DR	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20110119	N/A	ANDA	ANDA090970	Advanced Rx Pharmacy of Tennessee, LLC	PANTOPRAZOLE SODIUM	20 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0179-3)
0378-6689-10	0378-6689	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	pantoprazole sodium	TABLET, DELAYED RELEASE	ORAL	20110119	N/A	ANDA	ANDA090970	Mylan Pharmaceuticals Inc.	PANTOPRAZOLE SODIUM	40 mg/1	1000 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (0378-6689-10)
0378-6689-77	0378-6689	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	pantoprazole sodium	TABLET, DELAYED RELEASE	ORAL	20110119	N/A	ANDA	ANDA090970	Mylan Pharmaceuticals Inc.	PANTOPRAZOLE SODIUM	40 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (0378-6689-77)
51079-051-20	51079-051	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	pantoprazole sodium	TABLET, DELAYED RELEASE	ORAL	20110223	N/A	ANDA	ANDA090970	Mylan Institutional Inc.	PANTOPRAZOLE SODIUM	40 mg/1	100 BLISTER PACK in 1 CARTON (51079-051-20) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (51079-051-01)