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
65862-700-60	65862-700	HUMAN PRESCRIPTION DRUG	Cefuroxime Axetil	Cefuroxime Axetil	TABLET	ORAL	20060329	N/A	ANDA	ANDA065308	Aurobindo Pharma Limited	CEFUROXIME AXETIL	500 mg/1	60 TABLET in 1 BOTTLE (65862-700-60)
67296-2079-1	67296-2079	HUMAN PRESCRIPTION DRUG	Cefuroxime Axetil	Cefuroxime Axetil	TABLET, FILM COATED	ORAL	20060329	N/A	ANDA	ANDA065308	Redpharm Drug	CEFUROXIME AXETIL	500 mg/1	14 TABLET, FILM COATED in 1 BOTTLE (67296-2079-1)
57237-059-20	57237-059	HUMAN PRESCRIPTION DRUG	Cefuroxime Axetil	Cefuroxime Axetil	TABLET, FILM COATED	ORAL	20060329	N/A	ANDA	ANDA065308	Rising Pharma Holdings, Inc.	CEFUROXIME AXETIL	500 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (57237-059-20)
57237-059-60	57237-059	HUMAN PRESCRIPTION DRUG	Cefuroxime Axetil	Cefuroxime Axetil	TABLET, FILM COATED	ORAL	20060329	N/A	ANDA	ANDA065308	Rising Pharma Holdings, Inc.	CEFUROXIME AXETIL	500 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (57237-059-60)
68071-2958-2	68071-2958	HUMAN PRESCRIPTION DRUG	Cefuroxime Axetil	Cefuroxime Axetil	TABLET, FILM COATED	ORAL	20230320	N/A	ANDA	ANDA065308	NuCare Pharmaceuticals,Inc.	CEFUROXIME AXETIL	500 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (68071-2958-2)