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
63187-654-30	63187-654	HUMAN PRESCRIPTION DRUG	PANTOPRAZOLE SODIUM	PANTOPRAZOLE	TABLET, DELAYED RELEASE	ORAL	20181201	N/A	ANDA	ANDA202882	Proficient Rx LP	PANTOPRAZOLE SODIUM	40 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-654-30)
63187-654-90	63187-654	HUMAN PRESCRIPTION DRUG	PANTOPRAZOLE SODIUM	PANTOPRAZOLE	TABLET, DELAYED RELEASE	ORAL	20181201	N/A	ANDA	ANDA202882	Proficient Rx LP	PANTOPRAZOLE SODIUM	40 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-654-90)
31722-713-10	31722-713	HUMAN PRESCRIPTION DRUG	PANTOPRAZOLE SODIUM	PANTOPRAZOLE	TABLET, DELAYED RELEASE	ORAL	20140910	N/A	ANDA	ANDA202882	Camber Pharmaceuticals, Inc.	PANTOPRAZOLE SODIUM	40 mg/1	1000 TABLET, DELAYED RELEASE in 1 BOTTLE (31722-713-10)
31722-713-31	31722-713	HUMAN PRESCRIPTION DRUG	PANTOPRAZOLE SODIUM	PANTOPRAZOLE	TABLET, DELAYED RELEASE	ORAL	20140910	N/A	ANDA	ANDA202882	Camber Pharmaceuticals, Inc.	PANTOPRAZOLE SODIUM	40 mg/1	10 TABLET, DELAYED RELEASE in 1 BLISTER PACK (31722-713-31)
31722-713-32	31722-713	HUMAN PRESCRIPTION DRUG	PANTOPRAZOLE SODIUM	PANTOPRAZOLE	TABLET, DELAYED RELEASE	ORAL	20140910	N/A	ANDA	ANDA202882	Camber Pharmaceuticals, Inc.	PANTOPRAZOLE SODIUM	40 mg/1	10 TABLET, DELAYED RELEASE in 1 CARTON (31722-713-32)
31722-713-90	31722-713	HUMAN PRESCRIPTION DRUG	PANTOPRAZOLE SODIUM	PANTOPRAZOLE	TABLET, DELAYED RELEASE	ORAL	20140910	N/A	ANDA	ANDA202882	Camber Pharmaceuticals, Inc.	PANTOPRAZOLE SODIUM	40 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (31722-713-90)
76420-668-10	76420-668	HUMAN PRESCRIPTION DRUG	PANTOPRAZOLE SODIUM	PANTOPRAZOLE	TABLET, DELAYED RELEASE	ORAL	20240214	N/A	ANDA	ANDA202882	Asclemed USA, Inc.	PANTOPRAZOLE SODIUM	20 mg/1	10 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-668-10)
76420-668-30	76420-668	HUMAN PRESCRIPTION DRUG	PANTOPRAZOLE SODIUM	PANTOPRAZOLE	TABLET, DELAYED RELEASE	ORAL	20240214	N/A	ANDA	ANDA202882	Asclemed USA, Inc.	PANTOPRAZOLE SODIUM	20 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-668-30)
76420-668-60	76420-668	HUMAN PRESCRIPTION DRUG	PANTOPRAZOLE SODIUM	PANTOPRAZOLE	TABLET, DELAYED RELEASE	ORAL	20240214	N/A	ANDA	ANDA202882	Asclemed USA, Inc.	PANTOPRAZOLE SODIUM	20 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-668-60)
76420-668-90	76420-668	HUMAN PRESCRIPTION DRUG	PANTOPRAZOLE SODIUM	PANTOPRAZOLE	TABLET, DELAYED RELEASE	ORAL	20240214	N/A	ANDA	ANDA202882	Asclemed USA, Inc.	PANTOPRAZOLE SODIUM	20 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-668-90)
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)
72865-230-10	72865-230	HUMAN PRESCRIPTION DRUG	PANTOPRAZOLE SODIUM	PANTOPRAZOLE	TABLET, DELAYED RELEASE	ORAL	20220501	N/A	ANDA	ANDA202882	XLCare Pharmaceuticals Inc.	PANTOPRAZOLE SODIUM	40 mg/1	1000 TABLET, DELAYED RELEASE in 1 BOTTLE (72865-230-10)
72865-230-90	72865-230	HUMAN PRESCRIPTION DRUG	PANTOPRAZOLE SODIUM	PANTOPRAZOLE	TABLET, DELAYED RELEASE	ORAL	20220501	N/A	ANDA	ANDA202882	XLCare Pharmaceuticals Inc.	PANTOPRAZOLE SODIUM	40 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (72865-230-90)
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)