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)
检索条件:" 注册申请号=ANDA065308"
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
50090-4153-0 50090-4153 HUMAN PRESCRIPTION DRUG Cefuroxime Axetil Cefuroxime Axetil TABLET ORAL 20190222 N/A ANDA ANDA065308 A-S Medication Solutions CEFUROXIME AXETIL 500 mg/1 20 TABLET in 1 BOTTLE (50090-4153-0)
65862-698-20 65862-698 HUMAN PRESCRIPTION DRUG Cefuroxime Axetil Cefuroxime Axetil TABLET ORAL 20060329 N/A ANDA ANDA065308 Aurobindo Pharma Limited CEFUROXIME AXETIL 125 mg/1 20 TABLET in 1 BOTTLE (65862-698-20)
65862-698-60 65862-698 HUMAN PRESCRIPTION DRUG Cefuroxime Axetil Cefuroxime Axetil TABLET ORAL 20060329 N/A ANDA ANDA065308 Aurobindo Pharma Limited CEFUROXIME AXETIL 125 mg/1 60 TABLET in 1 BOTTLE (65862-698-60)
65862-699-20 65862-699 HUMAN PRESCRIPTION DRUG Cefuroxime Axetil Cefuroxime Axetil TABLET ORAL 20060329 N/A ANDA ANDA065308 Aurobindo Pharma Limited CEFUROXIME AXETIL 250 mg/1 20 TABLET in 1 BOTTLE (65862-699-20)
65862-699-60 65862-699 HUMAN PRESCRIPTION DRUG Cefuroxime Axetil Cefuroxime Axetil TABLET ORAL 20060329 N/A ANDA ANDA065308 Aurobindo Pharma Limited CEFUROXIME AXETIL 250 mg/1 60 TABLET in 1 BOTTLE (65862-699-60)
65862-700-20 65862-700 HUMAN PRESCRIPTION DRUG Cefuroxime Axetil Cefuroxime Axetil TABLET ORAL 20060329 N/A ANDA ANDA065308 Aurobindo Pharma Limited CEFUROXIME AXETIL 500 mg/1 20 TABLET in 1 BOTTLE (65862-700-20)
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)
16714-401-02 16714-401 HUMAN PRESCRIPTION DRUG Cefuroxime Axetil Cefuroxime Axetil TABLET ORAL 20060329 N/A ANDA ANDA065308 NorthStar Rx LLC CEFUROXIME AXETIL 500 mg/1 60 TABLET in 1 BOTTLE (16714-401-02)
68071-3899-4 68071-3899 HUMAN PRESCRIPTION DRUG Cefuroxime Axetil Cefuroxime Axetil TABLET, FILM COATED ORAL 20250924 N/A ANDA ANDA065308 NuCare Pharmaceuticals, Inc. CEFUROXIME AXETIL 500 mg/1 14 TABLET, FILM COATED in 1 BOTTLE (68071-3899-4)
68788-8905-2 68788-8905 HUMAN PRESCRIPTION DRUG Cefuroxime Axetil Cefuroxime Axetil TABLET, FILM COATED ORAL 20250731 N/A ANDA ANDA065308 Preferred Pharmaceuticals Inc. CEFUROXIME AXETIL 500 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (68788-8905-2)
43063-623-14 43063-623 HUMAN PRESCRIPTION DRUG Cefuroxime Axetil Cefuroxime Axetil TABLET ORAL 20241010 N/A ANDA ANDA065308 PD-Rx Pharmaceuticals, Inc. CEFUROXIME AXETIL 250 mg/1 14 TABLET in 1 BOTTLE, PLASTIC (43063-623-14)
43063-623-20 43063-623 HUMAN PRESCRIPTION DRUG Cefuroxime Axetil Cefuroxime Axetil TABLET ORAL 20151027 N/A ANDA ANDA065308 PD-Rx Pharmaceuticals, Inc. CEFUROXIME AXETIL 250 mg/1 20 TABLET in 1 BOTTLE, PLASTIC (43063-623-20)
43063-623-30 43063-623 HUMAN PRESCRIPTION DRUG Cefuroxime Axetil Cefuroxime Axetil TABLET ORAL 20151027 N/A ANDA ANDA065308 PD-Rx Pharmaceuticals, Inc. CEFUROXIME AXETIL 250 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (43063-623-30)
16714-401-01 16714-401 HUMAN PRESCRIPTION DRUG Cefuroxime Axetil Cefuroxime Axetil TABLET ORAL 20060329 N/A ANDA ANDA065308 NorthStar Rx LLC CEFUROXIME AXETIL 500 mg/1 20 TABLET in 1 BOTTLE (16714-401-01)
16714-400-02 16714-400 HUMAN PRESCRIPTION DRUG Cefuroxime Axetil Cefuroxime Axetil TABLET ORAL 20060329 N/A ANDA ANDA065308 NorthStar Rx LLC CEFUROXIME AXETIL 250 mg/1 60 TABLET in 1 BOTTLE (16714-400-02)
16714-400-01 16714-400 HUMAN PRESCRIPTION DRUG Cefuroxime Axetil Cefuroxime Axetil TABLET ORAL 20060329 N/A ANDA ANDA065308 NorthStar Rx LLC CEFUROXIME AXETIL 250 mg/1 20 TABLET in 1 BOTTLE (16714-400-01)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2026 Drugfuture->U.S. FDA National Drug Code DataBase