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
71335-0551-6	71335-0551	HUMAN PRESCRIPTION DRUG	PANTOPRAZOLE SODIUM	PANTOPRAZOLE	TABLET, DELAYED RELEASE	ORAL	20240403	N/A	ANDA	ANDA202882	Bryant Ranch Prepack	PANTOPRAZOLE SODIUM	40 mg/1	100 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0551-6)
71335-0551-7	71335-0551	HUMAN PRESCRIPTION DRUG	PANTOPRAZOLE SODIUM	PANTOPRAZOLE	TABLET, DELAYED RELEASE	ORAL	20240403	N/A	ANDA	ANDA202882	Bryant Ranch Prepack	PANTOPRAZOLE SODIUM	40 mg/1	10 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0551-7)
71335-0551-8	71335-0551	HUMAN PRESCRIPTION DRUG	PANTOPRAZOLE SODIUM	PANTOPRAZOLE	TABLET, DELAYED RELEASE	ORAL	20240403	N/A	ANDA	ANDA202882	Bryant Ranch Prepack	PANTOPRAZOLE SODIUM	40 mg/1	120 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0551-8)
71335-0551-9	71335-0551	HUMAN PRESCRIPTION DRUG	PANTOPRAZOLE SODIUM	PANTOPRAZOLE	TABLET, DELAYED RELEASE	ORAL	20240403	N/A	ANDA	ANDA202882	Bryant Ranch Prepack	PANTOPRAZOLE SODIUM	40 mg/1	180 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0551-9)
72189-112-30	72189-112	HUMAN PRESCRIPTION DRUG	PANTOPRAZOLE SODIUM	pantoprazole	TABLET, DELAYED RELEASE	ORAL	20200612	N/A	ANDA	ANDA202882	DIRECT RX	PANTOPRAZOLE SODIUM	20 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (72189-112-30)
72189-112-60	72189-112	HUMAN PRESCRIPTION DRUG	PANTOPRAZOLE SODIUM	pantoprazole	TABLET, DELAYED RELEASE	ORAL	20200612	N/A	ANDA	ANDA202882	DIRECT RX	PANTOPRAZOLE SODIUM	20 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (72189-112-60)
72189-112-90	72189-112	HUMAN PRESCRIPTION DRUG	PANTOPRAZOLE SODIUM	pantoprazole	TABLET, DELAYED RELEASE	ORAL	20200612	N/A	ANDA	ANDA202882	DIRECT RX	PANTOPRAZOLE SODIUM	20 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (72189-112-90)
71335-0551-2	71335-0551	HUMAN PRESCRIPTION DRUG	PANTOPRAZOLE SODIUM	PANTOPRAZOLE	TABLET, DELAYED RELEASE	ORAL	20200731	N/A	ANDA	ANDA202882	Bryant Ranch Prepack	PANTOPRAZOLE SODIUM	40 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0551-2)
71335-0551-3	71335-0551	HUMAN PRESCRIPTION DRUG	PANTOPRAZOLE SODIUM	PANTOPRAZOLE	TABLET, DELAYED RELEASE	ORAL	20200617	N/A	ANDA	ANDA202882	Bryant Ranch Prepack	PANTOPRAZOLE SODIUM	40 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0551-3)
71335-0551-4	71335-0551	HUMAN PRESCRIPTION DRUG	PANTOPRAZOLE SODIUM	PANTOPRAZOLE	TABLET, DELAYED RELEASE	ORAL	20240403	N/A	ANDA	ANDA202882	Bryant Ranch Prepack	PANTOPRAZOLE SODIUM	40 mg/1	58 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0551-4)
72865-229-90	72865-229	HUMAN PRESCRIPTION DRUG	PANTOPRAZOLE SODIUM	PANTOPRAZOLE	TABLET, DELAYED RELEASE	ORAL	20220501	N/A	ANDA	ANDA202882	XLCare Pharmaceuticals Inc.	PANTOPRAZOLE SODIUM	20 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (72865-229-90)
72865-230-10	72865-230	HUMAN PRESCRIPTION DRUG	PANTOPRAZOLE SODIUM	PANTOPRAZOLE	TABLET, DELAYED RELEASE	ORAL	20220501	N/A	ANDA	ANDA202882	XLCare Pharmaceuticals Inc.	PANTOPRAZOLE SODIUM	40 mg/1	1000 TABLET, DELAYED RELEASE in 1 BOTTLE (72865-230-10)
72865-230-90	72865-230	HUMAN PRESCRIPTION DRUG	PANTOPRAZOLE SODIUM	PANTOPRAZOLE	TABLET, DELAYED RELEASE	ORAL	20220501	N/A	ANDA	ANDA202882	XLCare Pharmaceuticals Inc.	PANTOPRAZOLE SODIUM	40 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (72865-230-90)