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
68788-7459-6	68788-7459	HUMAN PRESCRIPTION DRUG	Rabeprazole Sodium	Rabeprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20191227	N/A	ANDA	ANDA208644	Preferred Pharmaceuticals, Inc.	RABEPRAZOLE SODIUM	20 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-7459-6)
67877-443-30	67877-443	HUMAN PRESCRIPTION DRUG	Rabeprazole Sodium	Rabeprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20180427	N/A	ANDA	ANDA208644	Ascend Laboratories, LLC	RABEPRAZOLE SODIUM	20 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (67877-443-30)
67877-443-38	67877-443	HUMAN PRESCRIPTION DRUG	Rabeprazole Sodium	Rabeprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20180427	N/A	ANDA	ANDA208644	Ascend Laboratories, LLC	RABEPRAZOLE SODIUM	20 mg/1	100 POUCH in 1 CARTON (67877-443-38) / 1 BLISTER PACK in 1 POUCH / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK (67877-443-33)
67877-443-90	67877-443	HUMAN PRESCRIPTION DRUG	Rabeprazole Sodium	Rabeprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20180427	N/A	ANDA	ANDA208644	Ascend Laboratories, LLC	RABEPRAZOLE SODIUM	20 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (67877-443-90)
50090-4751-0	50090-4751	HUMAN PRESCRIPTION DRUG	Rabeprazole Sodium	Rabeprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20191125	N/A	ANDA	ANDA208644	A-S Medication Solutions	RABEPRAZOLE SODIUM	20 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-4751-0)
50090-4751-1	50090-4751	HUMAN PRESCRIPTION DRUG	Rabeprazole Sodium	Rabeprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20191125	N/A	ANDA	ANDA208644	A-S Medication Solutions	RABEPRAZOLE SODIUM	20 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-4751-1)
55700-767-30	55700-767	HUMAN PRESCRIPTION DRUG	Rabeprazole Sodium	Rabeprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20190621	N/A	ANDA	ANDA208644	Quality Care Products, LLC	RABEPRAZOLE SODIUM	20 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (55700-767-30)
55700-767-60	55700-767	HUMAN PRESCRIPTION DRUG	Rabeprazole Sodium	Rabeprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20190621	N/A	ANDA	ANDA208644	Quality Care Products, LLC	RABEPRAZOLE SODIUM	20 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (55700-767-60)
71205-292-90	71205-292	HUMAN PRESCRIPTION DRUG	Rabeprazole Sodium	Rabeprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20190701	N/A	ANDA	ANDA208644	Proficient Rx LP	RABEPRAZOLE SODIUM	20 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-292-90)