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
80425-0070-3	80425-0070	HUMAN PRESCRIPTION DRUG	Omeprazole DR	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20141031	N/A	ANDA	ANDA091672	Advanced Rx of Tennessee, LLC	OMEPRAZOLE	20 mg/1	120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0070-3)
80425-0070-4	80425-0070	HUMAN PRESCRIPTION DRUG	Omeprazole DR	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20141031	N/A	ANDA	ANDA091672	Advanced Rx of Tennessee, LLC	OMEPRAZOLE	20 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0070-4)
80425-0169-1	80425-0169	HUMAN PRESCRIPTION DRUG	Omeprazole DR	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20141031	N/A	ANDA	ANDA091672	Advanced Rx Pharmacy of Tennessee, LLC	OMEPRAZOLE	40 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0169-1)
80425-0169-2	80425-0169	HUMAN PRESCRIPTION DRUG	Omeprazole DR	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20141031	N/A	ANDA	ANDA091672	Advanced Rx Pharmacy of Tennessee, LLC	OMEPRAZOLE	40 mg/1	60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0169-2)