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
71335-0551-3	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)
71335-0551-5	71335-0551	HUMAN PRESCRIPTION DRUG	PANTOPRAZOLE SODIUM	PANTOPRAZOLE	TABLET, DELAYED RELEASE	ORAL	20220310	N/A	ANDA	ANDA202882	Bryant Ranch Prepack	PANTOPRAZOLE SODIUM	40 mg/1	14 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0551-5)
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)
63187-654-30	63187-654	HUMAN PRESCRIPTION DRUG	PANTOPRAZOLE SODIUM	PANTOPRAZOLE	TABLET, DELAYED RELEASE	ORAL	20181201	N/A	ANDA	ANDA202882	Proficient Rx LP	PANTOPRAZOLE SODIUM	40 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-654-30)
63187-654-90	63187-654	HUMAN PRESCRIPTION DRUG	PANTOPRAZOLE SODIUM	PANTOPRAZOLE	TABLET, DELAYED RELEASE	ORAL	20181201	N/A	ANDA	ANDA202882	Proficient Rx LP	PANTOPRAZOLE SODIUM	40 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-654-90)
82009-010-90	82009-010	HUMAN PRESCRIPTION DRUG	PANTOPRAZOLE SODIUM	PANTOPRAZOLE	TABLET, DELAYED RELEASE	ORAL	20220606	N/A	ANDA	ANDA202882	Quallent Pharmaceuticals Health LLC	PANTOPRAZOLE SODIUM	20 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (82009-010-90)
80425-0278-2	80425-0278	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium DR	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20230228	N/A	ANDA	ANDA202882	Advanced Rx Pharmacy of Tennessee, LLC	PANTOPRAZOLE SODIUM	20 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0278-2)
80425-0278-3	80425-0278	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium DR	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20230228	N/A	ANDA	ANDA202882	Advanced Rx Pharmacy of Tennessee, LLC	PANTOPRAZOLE SODIUM	20 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0278-3)