欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号NL/H/0859/002
药品名称Cofact 500 IU
活性成分
    • blood coagulation factors II, VII, IX, X in combination (Prothrombin complex) 0.0 IU/ml
剂型Powder and solvent for solution for injection
上市许可持有人Sanquin Plesmanlaan 125 1066 CX Amsterdam The Netherlands
参考成员国 - 产品名称Netherlands (NL)
Cofact
互认成员国 - 产品名称
    • Italy (IT)
    • Sweden (SE)
    • Iceland (IS)
    • Germany (DE)
      PEI.H.03453.02.1
    • Belgium (BE)
    • Luxembourg (LU)
    • Austria (AT)
      Cofact 500 I.E. Prothrombinkomplex vom Menschen, 250 I.E. Faktor IX pro Durchstechflasche Pulver ...
    • France (FR)
    • Finland (FI)
    • Spain (ES)
许可日期2006/11/19
最近更新日期2025/09/11
药物ATC编码
    • B02BD01 coagulation factor IX, II, VII and X in combination
申请类型
  • TypeLevel1：Known Active Substance
  • TypeLevel2：Initial Application
  • TypeLevel3：Biblio Art 10 a Dir 2001/83/EC
  • TypeLevel4：Biological: Blood Product
  • TypeLevel5：Prescription Only
附件文件下载
市场状态Positive
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