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
71610-003-60	71610-003	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20170808	N/A	ANDA	ANDA202038	Aphena Pharma Solutions - Tennessee, LLC	PANTOPRAZOLE SODIUM	40 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (71610-003-60)
71335-1165-6	71335-1165	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20240517	N/A	ANDA	ANDA202038	Bryant Ranch Prepack	PANTOPRAZOLE SODIUM	20 mg/1	10 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1165-6)
71335-1165-7	71335-1165	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20240517	N/A	ANDA	ANDA202038	Bryant Ranch Prepack	PANTOPRAZOLE SODIUM	20 mg/1	120 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1165-7)
71335-1165-8	71335-1165	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20240517	N/A	ANDA	ANDA202038	Bryant Ranch Prepack	PANTOPRAZOLE SODIUM	20 mg/1	180 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1165-8)
76420-805-10	76420-805	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20240501	N/A	ANDA	ANDA202038	Asclemed USA, Inc.	PANTOPRAZOLE SODIUM	20 mg/1	10 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-805-10)
76420-805-30	76420-805	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20240501	N/A	ANDA	ANDA202038	Asclemed USA, Inc.	PANTOPRAZOLE SODIUM	20 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-805-30)
76420-805-60	76420-805	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20240501	N/A	ANDA	ANDA202038	Asclemed USA, Inc.	PANTOPRAZOLE SODIUM	20 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-805-60)
76420-805-90	76420-805	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20240501	N/A	ANDA	ANDA202038	Asclemed USA, Inc.	PANTOPRAZOLE SODIUM	20 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-805-90)
50090-5361-0	50090-5361	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20201113	N/A	ANDA	ANDA202038	A-S Medication Solutions	PANTOPRAZOLE SODIUM	20 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-5361-0)
50090-5361-1	50090-5361	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20201113	N/A	ANDA	ANDA202038	A-S Medication Solutions	PANTOPRAZOLE SODIUM	20 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-5361-1)
50090-5361-2	50090-5361	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20201113	N/A	ANDA	ANDA202038	A-S Medication Solutions	PANTOPRAZOLE SODIUM	20 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-5361-2)