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
62135-534-08	62135-534	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20230405	N/A	ANDA	ANDA078281	Chartwell RX, LLC	PANTOPRAZOLE SODIUM	40 mg/1	450 TABLET, DELAYED RELEASE in 1 BOTTLE (62135-534-08)
62175-617-46	62175-617	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20110120	N/A	ANDA	ANDA078281	Lannett Company, Inc.	PANTOPRAZOLE SODIUM	40 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (62175-617-46)
62175-617-43	62175-617	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20110120	N/A	ANDA	ANDA078281	Lannett Company, Inc.	PANTOPRAZOLE SODIUM	40 mg/1	1000 TABLET, DELAYED RELEASE in 1 BOTTLE (62175-617-43)
62175-618-43	62175-618	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20110120	N/A	ANDA	ANDA078281	Lannett Company, Inc.	PANTOPRAZOLE SODIUM	20 mg/1	1000 TABLET, DELAYED RELEASE in 1 BOTTLE (62175-618-43)
62175-618-46	62175-618	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20110120	N/A	ANDA	ANDA078281	Lannett Company, Inc.	PANTOPRAZOLE SODIUM	20 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (62175-618-46)