欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号DE/H/0464/001
药品名称Octaplex 500
活性成分
    • blood coagulation factors II, VII, IX, X in combination (Prothrombin complex) 500.0 IU
剂型Powder and solvent for solution for infusion
上市许可持有人Octapharma GmbH Elisabeth-Selbert-Str. 11 D40764 Langenfeld Germany
参考成员国 - 产品名称Germany (DE)
Octaplex 500
互认成员国 - 产品名称
    • Iceland (IS)
    • Malta (MT)
      Octaplex 500 IU powder and solvent for solution for infusion
    • Ireland (IE)
    • Austria (AT)
      Octaplex 500 I.E. Pulver und Lösungsmittel zur Herstellung einer Infusionslösung
    • Cyprus (CY)
      Octaplex 500 IU powder and solvent for solution for infusion
    • France (FR)
    • Spain (ES)
    • Portugal (PT)
      Octaplex
    • Italy (IT)
    • Sweden (SE)
    • Norway (NO)
    • Finland (FI)
    • Poland (PL)
      Octaplex
    • Latvia (LV)
      Octaplex pulveris un šķīdinātājs infūziju šķīduma pagatavošanai
    • Lithuania (LT)
      OCTAPLEX 500 TV milteliai ir tirpiklis infuziniam tirpalui
    • Estonia (EE)
      OCTAPLEX
    • Hungary (HU)
    • Bulgaria (BG)
    • Czechia (CZ)
    • Romania (RO)
      PRONATIV 500 UI, pulbere şi solvent pentru soluţie perfuzabilă
    • Slovakia (SK)
      Octaplex
    • Slovenia (SI)
    • Denmark (DK)
    • United Kingdom (Northern Ireland) (XI)
    • Belgium (BE)
    • Netherlands (NL)
    • Luxembourg (LU)
许可日期2004/04/30
最近更新日期2024/04/12
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:Full Dossier Article 4.8 Di 65/65
  • TypeLevel4:Biological: Blood Product
  • TypeLevel5:Prescription Only
附件文件下载
市场状态Positive
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