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
68180-302-20	68180-302	HUMAN PRESCRIPTION DRUG	cefuroxime axetil	cefuroxime axetil	TABLET	ORAL	20081008	20250430	ANDA	ANDA065135	Lupin Pharmaceuticals, Inc.	CEFUROXIME AXETIL	250 mg/1	20 TABLET in 1 BOTTLE (68180-302-20)
68180-302-60	68180-302	HUMAN PRESCRIPTION DRUG	cefuroxime axetil	cefuroxime axetil	TABLET	ORAL	20081008	20250430	ANDA	ANDA065135	Lupin Pharmaceuticals, Inc.	CEFUROXIME AXETIL	250 mg/1	60 TABLET in 1 BOTTLE (68180-302-60)
43063-584-20	43063-584	HUMAN PRESCRIPTION DRUG	cefuroxime axetil	cefuroxime axetil	TABLET	ORAL	20141201	20250430	ANDA	ANDA065135	PD-Rx Pharmaceuticals, Inc.	CEFUROXIME AXETIL	250 mg/1	20 TABLET in 1 BOTTLE, PLASTIC (43063-584-20)
57297-302-20	57297-302	HUMAN PRESCRIPTION DRUG	cefuroxime axetil	cefuroxime axetil	TABLET	ORAL	20030725	20250430	ANDA	ANDA065135	LUPIN LIMITED	CEFUROXIME AXETIL	250 mg/1	20 TABLET in 1 BOTTLE (57297-302-20)
57297-302-60	57297-302	HUMAN PRESCRIPTION DRUG	cefuroxime axetil	cefuroxime axetil	TABLET	ORAL	20030725	20250430	ANDA	ANDA065135	LUPIN LIMITED	CEFUROXIME AXETIL	250 mg/1	60 TABLET in 1 BOTTLE (57297-302-60)
67296-0939-1	67296-0939	HUMAN PRESCRIPTION DRUG	cefuroxime axetil	cefuroxime axetil	TABLET	ORAL	20081008	20250430	ANDA	ANDA065135	RedPharm Drug	CEFUROXIME AXETIL	250 mg/1	20 TABLET in 1 BOTTLE (67296-0939-1)