欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号DE/H/0478/003
药品名称Haemoctin SDH 1000
活性成分
    • blood coagulation factor VIII human 1000.0 IU
剂型Powder and solvent for solution for injection
上市许可持有人Biotest Pharma GmbH Landsteiner Str. 5 D-63303 Dreieich Germany
参考成员国 - 产品名称Germany (DE)
Haemoctin SDH 1000
互认成员国 - 产品名称
    • United Kingdom (Northern Ireland) (XI)
    • Italy (IT)
    • Spain (ES)
    • Austria (AT)
      Haemoctin SDH 100 I.E./ml Pulver und Lösungsmittel zur Herstellung einer Injektionslösung
    • Greece (GR)
    • Poland (PL)
      Haemoctin 1000
    • Hungary (HU)
      HAEMOCTIN 1000 NE por és oldószer oldatos injekcióhoz
    • Bulgaria (BG)
    • Czechia (CZ)
    • Romania (RO)
      Haemoctin SDH 1000, pulbere şi solvent pentru soluţie injectabilă
    • Malta (MT)
许可日期2008/03/18
最近更新日期2024/09/27
药物ATC编码
    • B02BD02 coagulation factor VIII
申请类型
  • TypeLevel1:Known Active Substance
  • TypeLevel2:Additional Strength/Form
  • TypeLevel3:Full Dossier Art 8.3(i) 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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