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
85509-1443-9	85509-1443	HUMAN PRESCRIPTION DRUG	Rabeprazole Sodium	Rabeprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20250717	N/A	ANDA	ANDA208644	PHOENIX RX LLC	RABEPRAZOLE SODIUM	20 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (85509-1443-9)
60760-560-07	60760-560	HUMAN PRESCRIPTION DRUG	Rabeprazole Sodium	Rabeprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20241030	N/A	ANDA	ANDA208644	St. Mary's Medical Park Pharmacy	RABEPRAZOLE SODIUM	20 mg/1	7 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-560-07)
60760-560-30	60760-560	HUMAN PRESCRIPTION DRUG	Rabeprazole Sodium	Rabeprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20190910	N/A	ANDA	ANDA208644	St. Mary's Medical Park Pharmacy	RABEPRAZOLE SODIUM	20 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-560-30)
60760-560-60	60760-560	HUMAN PRESCRIPTION DRUG	Rabeprazole Sodium	Rabeprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20251104	N/A	ANDA	ANDA208644	St. Mary's Medical Park Pharmacy	RABEPRAZOLE SODIUM	20 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-560-60)
85509-1443-6	85509-1443	HUMAN PRESCRIPTION DRUG	Rabeprazole Sodium	Rabeprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20250717	N/A	ANDA	ANDA208644	PHOENIX RX LLC	RABEPRAZOLE SODIUM	20 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (85509-1443-6)
68788-7459-3	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	30 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-7459-3)
76420-818-90	76420-818	HUMAN PRESCRIPTION DRUG	Rabeprazole Sodium	Rabeprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20240625	N/A	ANDA	ANDA208644	Asclemed USA, Inc.	RABEPRAZOLE SODIUM	20 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-818-90)
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)
76420-818-30	76420-818	HUMAN PRESCRIPTION DRUG	Rabeprazole Sodium	Rabeprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20240625	N/A	ANDA	ANDA208644	Asclemed USA, Inc.	RABEPRAZOLE SODIUM	20 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-818-30)
76420-818-60	76420-818	HUMAN PRESCRIPTION DRUG	Rabeprazole Sodium	Rabeprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20240625	N/A	ANDA	ANDA208644	Asclemed USA, Inc.	RABEPRAZOLE SODIUM	20 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-818-60)
71335-1100-4	71335-1100	HUMAN PRESCRIPTION DRUG	Rabeprazole Sodium	Rabeprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20190307	N/A	ANDA	ANDA208644	Bryant Ranch Prepack	RABEPRAZOLE SODIUM	20 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1100-4)
71335-1100-6	71335-1100	HUMAN PRESCRIPTION DRUG	Rabeprazole Sodium	Rabeprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20240402	N/A	ANDA	ANDA208644	Bryant Ranch Prepack	RABEPRAZOLE SODIUM	20 mg/1	120 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1100-6)
71335-1100-2	71335-1100	HUMAN PRESCRIPTION DRUG	Rabeprazole Sodium	Rabeprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20210217	N/A	ANDA	ANDA208644	Bryant Ranch Prepack	RABEPRAZOLE SODIUM	20 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1100-2)
71335-1100-5	71335-1100	HUMAN PRESCRIPTION DRUG	Rabeprazole Sodium	Rabeprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20240402	N/A	ANDA	ANDA208644	Bryant Ranch Prepack	RABEPRAZOLE SODIUM	20 mg/1	28 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1100-5)
71335-1100-3	71335-1100	HUMAN PRESCRIPTION DRUG	Rabeprazole Sodium	Rabeprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20190208	N/A	ANDA	ANDA208644	Bryant Ranch Prepack	RABEPRAZOLE SODIUM	20 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1100-3)
72162-2367-5	72162-2367	HUMAN PRESCRIPTION DRUG	Rabeprazole Sodium	Rabeprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20240716	N/A	ANDA	ANDA208644	Bryant Ranch Prepack	RABEPRAZOLE SODIUM	20 mg/1	500 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-2367-5)