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
42291-765-90	42291-765	HUMAN PRESCRIPTION DRUG	PANTOPRAZOLE SODIUM	pantoprazole sodium	TABLET, DELAYED RELEASE	ORAL	20191021	N/A	ANDA	ANDA211368	AvKARE	PANTOPRAZOLE SODIUM	40 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (42291-765-90)
42291-765-10	42291-765	HUMAN PRESCRIPTION DRUG	PANTOPRAZOLE SODIUM	pantoprazole sodium	TABLET, DELAYED RELEASE	ORAL	20191021	N/A	ANDA	ANDA211368	AvKARE	PANTOPRAZOLE SODIUM	40 mg/1	1000 TABLET, DELAYED RELEASE in 1 BOTTLE (42291-765-10)
50742-151-90	50742-151	HUMAN PRESCRIPTION DRUG	PANTOPRAZOLE SODIUM	pantoprazole sodium	TABLET, DELAYED RELEASE	ORAL	20190311	N/A	ANDA	ANDA211368	Ingenus Pharmaceuticals, LLC	PANTOPRAZOLE SODIUM	40 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (50742-151-90)
50742-151-10	50742-151	HUMAN PRESCRIPTION DRUG	PANTOPRAZOLE SODIUM	pantoprazole sodium	TABLET, DELAYED RELEASE	ORAL	20190311	N/A	ANDA	ANDA211368	Ingenus Pharmaceuticals, LLC	PANTOPRAZOLE SODIUM	40 mg/1	1000 TABLET, DELAYED RELEASE in 1 BOTTLE (50742-151-10)