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
67296-1187-3	67296-1187	HUMAN PRESCRIPTION DRUG	PANTOPRAZOLE SODIUM	PANTOPRAZOLE	TABLET, DELAYED RELEASE	ORAL	20140910	N/A	ANDA	ANDA202882	RedPharm Drug	PANTOPRAZOLE SODIUM	20 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (67296-1187-3)
50090-5794-0	50090-5794	HUMAN PRESCRIPTION DRUG	PANTOPRAZOLE SODIUM	PANTOPRAZOLE	TABLET, DELAYED RELEASE	ORAL	20211011	N/A	ANDA	ANDA202882	A-S Medication Solutions	PANTOPRAZOLE SODIUM	40 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-5794-0)
50090-5794-1	50090-5794	HUMAN PRESCRIPTION DRUG	PANTOPRAZOLE SODIUM	PANTOPRAZOLE	TABLET, DELAYED RELEASE	ORAL	20211011	N/A	ANDA	ANDA202882	A-S Medication Solutions	PANTOPRAZOLE SODIUM	40 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-5794-1)
63187-831-30	63187-831	HUMAN PRESCRIPTION DRUG	PANTOPRAZOLE SODIUM	PANTOPRAZOLE	TABLET, DELAYED RELEASE	ORAL	20170403	N/A	ANDA	ANDA202882	Proficient Rx LP	PANTOPRAZOLE SODIUM	20 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-831-30)
63187-831-60	63187-831	HUMAN PRESCRIPTION DRUG	PANTOPRAZOLE SODIUM	PANTOPRAZOLE	TABLET, DELAYED RELEASE	ORAL	20170403	N/A	ANDA	ANDA202882	Proficient Rx LP	PANTOPRAZOLE SODIUM	20 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-831-60)
63187-831-90	63187-831	HUMAN PRESCRIPTION DRUG	PANTOPRAZOLE SODIUM	PANTOPRAZOLE	TABLET, DELAYED RELEASE	ORAL	20170403	N/A	ANDA	ANDA202882	Proficient Rx LP	PANTOPRAZOLE SODIUM	20 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-831-90)
68071-2285-6	68071-2285	HUMAN PRESCRIPTION DRUG	PANTOPRAZOLE SODIUM	PANTOPRAZOLE	TABLET, DELAYED RELEASE	ORAL	20201027	N/A	ANDA	ANDA202882	NuCare Pharmaceuticals,Inc.	PANTOPRAZOLE SODIUM	20 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-2285-6)
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)
50090-5793-0	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	60 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-5793-0)
50090-5793-1	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	90 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-5793-1)
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)
67046-0155-3	67046-0155	HUMAN PRESCRIPTION DRUG	PANTOPRAZOLE SODIUM	PANTOPRAZOLE	TABLET, DELAYED RELEASE	ORAL	20241106	N/A	ANDA	ANDA202882	Coupler LLC	PANTOPRAZOLE SODIUM	40 mg/1	30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (67046-0155-3)
53002-2419-3	53002-2419	HUMAN PRESCRIPTION DRUG	PANTOPRAZOLE SODIUM	PANTOPRAZOLE	TABLET, DELAYED RELEASE	ORAL	20220101	N/A	ANDA	ANDA202882	RPK Pharmaceuticals, Inc.	PANTOPRAZOLE SODIUM	40 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (53002-2419-3)
53002-2419-5	53002-2419	HUMAN PRESCRIPTION DRUG	PANTOPRAZOLE SODIUM	PANTOPRAZOLE	TABLET, DELAYED RELEASE	ORAL	20220101	N/A	ANDA	ANDA202882	RPK Pharmaceuticals, Inc.	PANTOPRAZOLE SODIUM	40 mg/1	15 TABLET, DELAYED RELEASE in 1 BOTTLE (53002-2419-5)
53002-2419-6	53002-2419	HUMAN PRESCRIPTION DRUG	PANTOPRAZOLE SODIUM	PANTOPRAZOLE	TABLET, DELAYED RELEASE	ORAL	20220101	N/A	ANDA	ANDA202882	RPK Pharmaceuticals, Inc.	PANTOPRAZOLE SODIUM	40 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (53002-2419-6)
53002-2419-9	53002-2419	HUMAN PRESCRIPTION DRUG	PANTOPRAZOLE SODIUM	PANTOPRAZOLE	TABLET, DELAYED RELEASE	ORAL	20220101	N/A	ANDA	ANDA202882	RPK Pharmaceuticals, Inc.	PANTOPRAZOLE SODIUM	40 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (53002-2419-9)
76420-669-10	76420-669	HUMAN PRESCRIPTION DRUG	PANTOPRAZOLE SODIUM	PANTOPRAZOLE	TABLET, DELAYED RELEASE	ORAL	20240214	N/A	ANDA	ANDA202882	Asclemed USA, Inc.	PANTOPRAZOLE SODIUM	40 mg/1	10 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-669-10)
76420-669-30	76420-669	HUMAN PRESCRIPTION DRUG	PANTOPRAZOLE SODIUM	PANTOPRAZOLE	TABLET, DELAYED RELEASE	ORAL	20240214	N/A	ANDA	ANDA202882	Asclemed USA, Inc.	PANTOPRAZOLE SODIUM	40 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-669-30)