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
71335-0310-7	71335-0310	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20220502	N/A	ANDA	ANDA202038	Bryant Ranch Prepack	PANTOPRAZOLE SODIUM	40 mg/1	10 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0310-7)
71335-0310-8	71335-0310	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20220502	N/A	ANDA	ANDA202038	Bryant Ranch Prepack	PANTOPRAZOLE SODIUM	40 mg/1	120 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0310-8)
71335-0310-9	71335-0310	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20220502	N/A	ANDA	ANDA202038	Bryant Ranch Prepack	PANTOPRAZOLE SODIUM	40 mg/1	180 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0310-9)
80425-0406-1	80425-0406	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium DR	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20240627	N/A	ANDA	ANDA202038	Advanced Rx of Tennessee, LLC	PANTOPRAZOLE SODIUM	20 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0406-1)
80425-0406-2	80425-0406	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium DR	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20240627	N/A	ANDA	ANDA202038	Advanced Rx of Tennessee, LLC	PANTOPRAZOLE SODIUM	20 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0406-2)
80425-0406-3	80425-0406	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium DR	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20240627	N/A	ANDA	ANDA202038	Advanced Rx of Tennessee, LLC	PANTOPRAZOLE SODIUM	20 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0406-3)
83008-034-30	83008-034	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20230718	N/A	ANDA	ANDA202038	Quality Care Products, LLC	PANTOPRAZOLE SODIUM	20 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (83008-034-30)
83008-034-60	83008-034	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20230718	N/A	ANDA	ANDA202038	Quality Care Products, LLC	PANTOPRAZOLE SODIUM	20 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (83008-034-60)
51655-075-25	51655-075	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20240223	N/A	ANDA	ANDA202038	Northwind Pharmaceuticals, LLC	PANTOPRAZOLE SODIUM	20 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (51655-075-25)
71335-0310-1	71335-0310	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20190307	N/A	ANDA	ANDA202038	Bryant Ranch Prepack	PANTOPRAZOLE SODIUM	40 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0310-1)
71335-0310-2	71335-0310	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20190313	N/A	ANDA	ANDA202038	Bryant Ranch Prepack	PANTOPRAZOLE SODIUM	40 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0310-2)