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
68071-4895-9	68071-4895	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20190515	N/A	ANDA	ANDA202038	NuCare Pharmaceuticals,Inc.	PANTOPRAZOLE SODIUM	40 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-4895-9)
68071-4917-4	68071-4917	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20190606	N/A	ANDA	ANDA202038	NuCare Pharmaceuticals,Inc.	PANTOPRAZOLE SODIUM	40 mg/1	14 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-4917-4)
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)
76420-806-10	76420-806	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20240501	N/A	ANDA	ANDA202038	Asclemed USA, Inc.	PANTOPRAZOLE SODIUM	40 mg/1	10 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-806-10)
76420-806-30	76420-806	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20240501	N/A	ANDA	ANDA202038	Asclemed USA, Inc.	PANTOPRAZOLE SODIUM	40 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-806-30)
76420-806-60	76420-806	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20240501	N/A	ANDA	ANDA202038	Asclemed USA, Inc.	PANTOPRAZOLE SODIUM	40 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-806-60)
76420-806-90	76420-806	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20240501	N/A	ANDA	ANDA202038	Asclemed USA, Inc.	PANTOPRAZOLE SODIUM	40 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-806-90)
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)
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)
0615-8113-05	0615-8113	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20221215	N/A	ANDA	ANDA202038	NCS HealthCare of KY, LLC dba Vangard Labs	PANTOPRAZOLE SODIUM	20 mg/1	15 TABLET, DELAYED RELEASE in 1 BLISTER PACK (0615-8113-05)
0615-8113-39	0615-8113	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20181107	N/A	ANDA	ANDA202038	NCS HealthCare of KY, LLC dba Vangard Labs	PANTOPRAZOLE SODIUM	20 mg/1	30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (0615-8113-39)
55154-4165-0	55154-4165	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20120928	N/A	ANDA	ANDA202038	Cardinal Health 107, LLC	PANTOPRAZOLE SODIUM	40 mg/1	10 BLISTER PACK in 1 BAG (55154-4165-0) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK
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)
76420-805-10	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)
68071-5053-6	68071-5053	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20190911	N/A	ANDA	ANDA202038	NuCare Pharmaceuticals,Inc.	PANTOPRAZOLE SODIUM	20 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-5053-6)
71335-1165-2	71335-1165	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20190321	N/A	ANDA	ANDA202038	Bryant Ranch Prepack	PANTOPRAZOLE SODIUM	20 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1165-2)
71335-1165-5	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	28 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1165-5)
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)