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
50090-5793-2	50090-5793	HUMAN PRESCRIPTION DRUG	PANTOPRAZOLE SODIUM	PANTOPRAZOLE	TABLET, DELAYED RELEASE	ORAL	20211011	N/A	ANDA	ANDA202882	A-S Medication Solutions	PANTOPRAZOLE SODIUM	20 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-5793-2)
76420-674-01	76420-674	HUMAN PRESCRIPTION DRUG	PANTOPRAZOLE SODIUM	PANTOPRAZOLE	TABLET, DELAYED RELEASE	ORAL	20240313	N/A	ANDA	ANDA202882	Asclemed USA, Inc.	PANTOPRAZOLE SODIUM	40 mg/1	100 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-674-01)
76420-674-10	76420-674	HUMAN PRESCRIPTION DRUG	PANTOPRAZOLE SODIUM	PANTOPRAZOLE	TABLET, DELAYED RELEASE	ORAL	20240313	N/A	ANDA	ANDA202882	Asclemed USA, Inc.	PANTOPRAZOLE SODIUM	40 mg/1	10 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-674-10)
76420-674-30	76420-674	HUMAN PRESCRIPTION DRUG	PANTOPRAZOLE SODIUM	PANTOPRAZOLE	TABLET, DELAYED RELEASE	ORAL	20240313	N/A	ANDA	ANDA202882	Asclemed USA, Inc.	PANTOPRAZOLE SODIUM	40 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-674-30)
51655-744-52	51655-744	HUMAN PRESCRIPTION DRUG	PANTOPRAZOLE SODIUM	PANTOPRAZOLE	TABLET, DELAYED RELEASE	ORAL	20210709	N/A	ANDA	ANDA202882	Northwind Health Company, LLC	PANTOPRAZOLE SODIUM	20 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (51655-744-52)
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)
76420-671-01	76420-671	HUMAN PRESCRIPTION DRUG	PANTOPRAZOLE SODIUM	PANTOPRAZOLE	TABLET, DELAYED RELEASE	ORAL	20240313	N/A	ANDA	ANDA202882	Asclemed USA, Inc.	PANTOPRAZOLE SODIUM	20 mg/1	100 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-671-01)
76420-671-10	76420-671	HUMAN PRESCRIPTION DRUG	PANTOPRAZOLE SODIUM	PANTOPRAZOLE	TABLET, DELAYED RELEASE	ORAL	20240313	N/A	ANDA	ANDA202882	Asclemed USA, Inc.	PANTOPRAZOLE SODIUM	20 mg/1	10 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-671-10)
76420-671-30	76420-671	HUMAN PRESCRIPTION DRUG	PANTOPRAZOLE SODIUM	PANTOPRAZOLE	TABLET, DELAYED RELEASE	ORAL	20240313	N/A	ANDA	ANDA202882	Asclemed USA, Inc.	PANTOPRAZOLE SODIUM	20 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-671-30)
76420-671-60	76420-671	HUMAN PRESCRIPTION DRUG	PANTOPRAZOLE SODIUM	PANTOPRAZOLE	TABLET, DELAYED RELEASE	ORAL	20240313	N/A	ANDA	ANDA202882	Asclemed USA, Inc.	PANTOPRAZOLE SODIUM	20 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-671-60)
76420-671-90	76420-671	HUMAN PRESCRIPTION DRUG	PANTOPRAZOLE SODIUM	PANTOPRAZOLE	TABLET, DELAYED RELEASE	ORAL	20240313	N/A	ANDA	ANDA202882	Asclemed USA, Inc.	PANTOPRAZOLE SODIUM	20 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-671-90)
76420-674-60	76420-674	HUMAN PRESCRIPTION DRUG	PANTOPRAZOLE SODIUM	PANTOPRAZOLE	TABLET, DELAYED RELEASE	ORAL	20240313	N/A	ANDA	ANDA202882	Asclemed USA, Inc.	PANTOPRAZOLE SODIUM	40 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-674-60)
76420-674-90	76420-674	HUMAN PRESCRIPTION DRUG	PANTOPRAZOLE SODIUM	PANTOPRAZOLE	TABLET, DELAYED RELEASE	ORAL	20240313	N/A	ANDA	ANDA202882	Asclemed USA, Inc.	PANTOPRAZOLE SODIUM	40 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-674-90)