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
45865-802-60	45865-802	HUMAN PRESCRIPTION DRUG	RABEPRAZOLE SODIUM	RABEPRAZOLE SODIUM	TABLET, DELAYED RELEASE	ORAL	20180601	N/A	ANDA	ANDA078964	medsource pharmaceuticals	RABEPRAZOLE SODIUM	20 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (45865-802-60)
63187-788-60	63187-788	HUMAN PRESCRIPTION DRUG	RABEPRAZOLE SODIUM	RABEPRAZOLE SODIUM	TABLET, DELAYED RELEASE	ORAL	20161201	N/A	ANDA	ANDA078964	Proficient Rx LP	RABEPRAZOLE SODIUM	20 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-788-60)
63187-788-90	63187-788	HUMAN PRESCRIPTION DRUG	RABEPRAZOLE SODIUM	RABEPRAZOLE SODIUM	TABLET, DELAYED RELEASE	ORAL	20131108	N/A	ANDA	ANDA078964	Proficient Rx LP	RABEPRAZOLE SODIUM	20 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-788-90)
63187-788-30	63187-788	HUMAN PRESCRIPTION DRUG	RABEPRAZOLE SODIUM	RABEPRAZOLE SODIUM	TABLET, DELAYED RELEASE	ORAL	20131108	N/A	ANDA	ANDA078964	Proficient Rx LP	RABEPRAZOLE SODIUM	20 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-788-30)
45865-802-30	45865-802	HUMAN PRESCRIPTION DRUG	RABEPRAZOLE SODIUM	RABEPRAZOLE SODIUM	TABLET, DELAYED RELEASE	ORAL	20180601	N/A	ANDA	ANDA078964	medsource pharmaceuticals	RABEPRAZOLE SODIUM	20 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (45865-802-30)