美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=CEFUROXIME"
商品名 申请号 产品号 申请类型 活性成分 剂型/给药途径 规格/剂量 RLD RS 申请号原始批准/暂定批准日期 产品号批准日期 申请人 市场状态
CEFUROXIME AXETIL 065323 002 ANDA CEFUROXIME AXETIL FOR SUSPENSION;ORAL EQ 250MG BASE/5ML No No 2008/02/05 2008/02/05 SUN PHARM INDS LTD Discontinued
CEFUROXIME AXETIL 065359 001 ANDA CEFUROXIME AXETIL TABLET;ORAL EQ 125MG BASE No No 2008/02/15 2008/02/15 ANDA REPOSITORY Prescription
CEFUROXIME AXETIL 065359 002 ANDA CEFUROXIME AXETIL TABLET;ORAL EQ 250MG BASE No No 2008/02/15 2008/02/15 ANDA REPOSITORY Prescription
CEFUROXIME AXETIL 065359 003 ANDA CEFUROXIME AXETIL TABLET;ORAL EQ 500MG BASE No No 2008/02/15 2008/02/15 ANDA REPOSITORY Prescription
CEFUROXIME SODIUM 065483 001 ANDA CEFUROXIME SODIUM INJECTABLE;INTRAMUSCULAR, INTRAVENOUS EQ 750MG BASE/VIAL No No 2008/10/15 2008/10/15 HOSPIRA INC Discontinued
CEFUROXIME SODIUM 065483 002 ANDA CEFUROXIME SODIUM INJECTABLE;INJECTION EQ 1.5GM BASE/VIAL No No 2008/10/15 2008/10/15 HOSPIRA INC Discontinued
CEFUROXIME SODIUM 065484 001 ANDA CEFUROXIME SODIUM INJECTABLE;INJECTION EQ 7.5GM BASE/VIAL No No 2008/10/15 2008/10/15 HOSPIRA INC Discontinued
CEFUROXIME SODIUM 065503 001 ANDA CEFUROXIME SODIUM INJECTABLE;INJECTION EQ 1.5GM BASE/VIAL No No 2008/10/15 2008/10/15 HOSPIRA INC Discontinued
CEFUROXIME SODIUM IN PLASTIC CONTAINER 065251 001 ANDA CEFUROXIME SODIUM INJECTABLE;INJECTION EQ 75GM BASE/VIAL No No 2009/12/30 2009/12/30 SAMSON MEDCL Discontinued
CEFUROXIME SODIUM IN PLASTIC CONTAINER 065251 002 ANDA CEFUROXIME SODIUM INJECTABLE;INJECTION EQ 225GM BASE/VIAL No No 2009/12/30 2009/12/30 SAMSON MEDCL Discontinued
CEFUROXIME AXETIL 065496 001 ANDA CEFUROXIME AXETIL TABLET;ORAL EQ 250MG BASE No No 2010/06/07 2010/06/07 ALKEM LABS LTD Prescription
CEFUROXIME AXETIL 065496 002 ANDA CEFUROXIME AXETIL TABLET;ORAL EQ 500MG BASE No No 2010/06/07 2010/06/07 ALKEM LABS LTD Prescription
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