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
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)
71335-0551-1	71335-0551	HUMAN PRESCRIPTION DRUG	PANTOPRAZOLE SODIUM	PANTOPRAZOLE	TABLET, DELAYED RELEASE	ORAL	20200915	N/A	ANDA	ANDA202882	Bryant Ranch Prepack	PANTOPRAZOLE SODIUM	40 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0551-1)
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)
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)
60760-679-30	60760-679	HUMAN PRESCRIPTION DRUG	PANTOPRAZOLE SODIUM	PANTOPRAZOLE	TABLET, DELAYED RELEASE	ORAL	20220301	N/A	ANDA	ANDA202882	St Mary's Medical Park Pharmacy	PANTOPRAZOLE SODIUM	40 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-679-30)
60760-712-60	60760-712	HUMAN PRESCRIPTION DRUG	PANTOPRAZOLE SODIUM	PANTOPRAZOLE	TABLET, DELAYED RELEASE	ORAL	20200304	N/A	ANDA	ANDA202882	St. Mary's Medical Park Pharmacy	PANTOPRAZOLE SODIUM	20 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-712-60)
68071-4864-9	68071-4864	HUMAN PRESCRIPTION DRUG	PANTOPRAZOLE SODIUM	PANTOPRAZOLE	TABLET, DELAYED RELEASE	ORAL	20190424	N/A	ANDA	ANDA202882	NuCare Pharmaceuticals,Inc.	PANTOPRAZOLE SODIUM	40 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-4864-9)