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
80425-0449-3	80425-0449	HUMAN PRESCRIPTION DRUG	RABEPRAZOLE SODIUM	rabeprazole sodium	TABLET, DELAYED RELEASE	ORAL	20241115	N/A	ANDA	ANDA204237	Advanced Rx of Tennessee, LLC	RABEPRAZOLE SODIUM	20 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0449-3)
80425-0449-1	80425-0449	HUMAN PRESCRIPTION DRUG	RABEPRAZOLE SODIUM	rabeprazole sodium	TABLET, DELAYED RELEASE	ORAL	20241115	N/A	ANDA	ANDA204237	Advanced Rx of Tennessee, LLC	RABEPRAZOLE SODIUM	20 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0449-1)
50090-6887-1	50090-6887	HUMAN PRESCRIPTION DRUG	RABEPRAZOLE SODIUM	rabeprazole sodium	TABLET, DELAYED RELEASE	ORAL	20231206	N/A	ANDA	ANDA204237	A-S Medication Solutions	RABEPRAZOLE SODIUM	20 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-6887-1)
50090-6887-0	50090-6887	HUMAN PRESCRIPTION DRUG	RABEPRAZOLE SODIUM	rabeprazole sodium	TABLET, DELAYED RELEASE	ORAL	20231206	N/A	ANDA	ANDA204237	A-S Medication Solutions	RABEPRAZOLE SODIUM	20 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-6887-0)
72888-059-30	72888-059	HUMAN PRESCRIPTION DRUG	RABEPRAZOLE SODIUM	rabeprazole sodium	TABLET, DELAYED RELEASE	ORAL	20170601	N/A	ANDA	ANDA204237	Advagen Pharma Limited	RABEPRAZOLE SODIUM	20 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (72888-059-30)
72888-059-90	72888-059	HUMAN PRESCRIPTION DRUG	RABEPRAZOLE SODIUM	rabeprazole sodium	TABLET, DELAYED RELEASE	ORAL	20170601	N/A	ANDA	ANDA204237	Advagen Pharma Limited	RABEPRAZOLE SODIUM	20 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (72888-059-90)
71205-603-30	71205-603	HUMAN PRESCRIPTION DRUG	RABEPRAZOLE SODIUM	rabeprazole sodium	TABLET, DELAYED RELEASE	ORAL	20210914	N/A	ANDA	ANDA204237	Proficient Rx LP	RABEPRAZOLE SODIUM	20 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-603-30)
71205-603-90	71205-603	HUMAN PRESCRIPTION DRUG	RABEPRAZOLE SODIUM	rabeprazole sodium	TABLET, DELAYED RELEASE	ORAL	20210914	N/A	ANDA	ANDA204237	Proficient Rx LP	RABEPRAZOLE SODIUM	20 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-603-90)
71205-603-60	71205-603	HUMAN PRESCRIPTION DRUG	RABEPRAZOLE SODIUM	rabeprazole sodium	TABLET, DELAYED RELEASE	ORAL	20210914	N/A	ANDA	ANDA204237	Proficient Rx LP	RABEPRAZOLE SODIUM	20 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-603-60)