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
70010-190-09	70010-190	HUMAN PRESCRIPTION DRUG	pantoprazole sodium	pantoprazole sodium	TABLET, DELAYED RELEASE	ORAL	20240412	N/A	ANDA	ANDA217282	Granules Pharmaceuticals Inc.	PANTOPRAZOLE SODIUM	20 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (70010-190-09)
70010-190-10	70010-190	HUMAN PRESCRIPTION DRUG	pantoprazole sodium	pantoprazole sodium	TABLET, DELAYED RELEASE	ORAL	20240412	N/A	ANDA	ANDA217282	Granules Pharmaceuticals Inc.	PANTOPRAZOLE SODIUM	20 mg/1	1000 TABLET, DELAYED RELEASE in 1 BOTTLE (70010-190-10)
70010-191-09	70010-191	HUMAN PRESCRIPTION DRUG	pantoprazole sodium	pantoprazole sodium	TABLET, DELAYED RELEASE	ORAL	20240412	N/A	ANDA	ANDA217282	Granules Pharmaceuticals Inc.	PANTOPRAZOLE SODIUM	40 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (70010-191-09)
70010-191-10	70010-191	HUMAN PRESCRIPTION DRUG	pantoprazole sodium	pantoprazole sodium	TABLET, DELAYED RELEASE	ORAL	20240412	N/A	ANDA	ANDA217282	Granules Pharmaceuticals Inc.	PANTOPRAZOLE SODIUM	40 mg/1	1000 TABLET, DELAYED RELEASE in 1 BOTTLE (70010-191-10)