美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件: 药品名称=KEFLEX
符合检索条件的记录共7
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1药品名称KEFLEX
申请号050405产品号002
活性成分CEPHALEXIN市场状态处方药
剂型或给药途径CAPSULE;ORAL规格EQ 250MG BASE
治疗等效代码AB参比药物
批准日期Approved Prior to Jan 1, 1982申请机构PRAGMA PHARMACEUTICALS LLC
2药品名称KEFLEX
申请号050405产品号003
活性成分CEPHALEXIN市场状态处方药
剂型或给药途径CAPSULE;ORAL规格EQ 500MG BASE
治疗等效代码AB参比药物
批准日期Approved Prior to Jan 1, 1982申请机构PRAGMA PHARMACEUTICALS LLC
3药品名称KEFLEX
申请号050405产品号004
活性成分CEPHALEXIN市场状态停止上市
剂型或给药途径CAPSULE;ORAL规格EQ 333MG BASE
治疗等效代码参比药物
批准日期2006/05/12申请机构PRAGMA PHARMACEUTICALS LLC
4药品名称KEFLEX
申请号050405产品号005
活性成分CEPHALEXIN市场状态处方药
剂型或给药途径CAPSULE;ORAL规格EQ 750MG BASE
治疗等效代码AB参比药物
批准日期2006/05/12申请机构PRAGMA PHARMACEUTICALS LLC
5药品名称KEFLEX
申请号050406产品号001
活性成分CEPHALEXIN市场状态停止上市
剂型或给药途径FOR SUSPENSION;ORAL规格EQ 125MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
治疗等效代码参比药物
批准日期Approved Prior to Jan 1, 1982申请机构PRAGMA PHARMACEUTICALS LLC
6药品名称KEFLEX
申请号050406产品号002
活性成分CEPHALEXIN市场状态停止上市
剂型或给药途径FOR SUSPENSION;ORAL规格EQ 250MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons*
治疗等效代码参比药物
批准日期Approved Prior to Jan 1, 1982申请机构PRAGMA PHARMACEUTICALS LLC
7药品名称KEFLEX
申请号050406产品号003
活性成分CEPHALEXIN市场状态停止上市
剂型或给药途径FOR SUSPENSION;ORAL规格EQ 100MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons*
治疗等效代码参比药物
批准日期Approved Prior to Jan 1, 1982申请机构PRAGMA PHARMACEUTICALS LLC