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
68788-8536-6	68788-8536	HUMAN PRESCRIPTION DRUG	RABEPRAZOLE SODIUM	rabeprazole sodium	TABLET, DELAYED RELEASE	ORAL	20231019	N/A	ANDA	ANDA204237	Preferred Pharmaceuticals Inc.	RABEPRAZOLE SODIUM	20 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-8536-6)
71335-2304-2	71335-2304	HUMAN PRESCRIPTION DRUG	RABEPRAZOLE SODIUM	rabeprazole sodium	TABLET, DELAYED RELEASE	ORAL	20231208	N/A	ANDA	ANDA204237	Bryant Ranch Prepack	RABEPRAZOLE SODIUM	20 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2304-2)
71335-2304-3	71335-2304	HUMAN PRESCRIPTION DRUG	RABEPRAZOLE SODIUM	rabeprazole sodium	TABLET, DELAYED RELEASE	ORAL	20231208	N/A	ANDA	ANDA204237	Bryant Ranch Prepack	RABEPRAZOLE SODIUM	20 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2304-3)
71335-2304-4	71335-2304	HUMAN PRESCRIPTION DRUG	RABEPRAZOLE SODIUM	rabeprazole sodium	TABLET, DELAYED RELEASE	ORAL	20231208	N/A	ANDA	ANDA204237	Bryant Ranch Prepack	RABEPRAZOLE SODIUM	20 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2304-4)
71335-2304-5	71335-2304	HUMAN PRESCRIPTION DRUG	RABEPRAZOLE SODIUM	rabeprazole sodium	TABLET, DELAYED RELEASE	ORAL	20231208	N/A	ANDA	ANDA204237	Bryant Ranch Prepack	RABEPRAZOLE SODIUM	20 mg/1	28 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2304-5)
71335-2304-6	71335-2304	HUMAN PRESCRIPTION DRUG	RABEPRAZOLE SODIUM	rabeprazole sodium	TABLET, DELAYED RELEASE	ORAL	20231208	N/A	ANDA	ANDA204237	Bryant Ranch Prepack	RABEPRAZOLE SODIUM	20 mg/1	120 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2304-6)