欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号DE/H/0216/002
药品名称Rabipur
活性成分
    • Rabies virus, inactivated 2.5 IU/ml
剂型POWDER AND SOLVENT FOR SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE
上市许可持有人Bavarian Nordic A/S Philip Heymans Allé 3 2900 Hellerup Denmark
参考成员国 - 产品名称Germany (DE)
Rabipur
互认成员国 - 产品名称
    • Denmark (DK)
    • Belgium (BE)
      Rabipur poeder en oplosmiddel voor oplossing voor injectie in een voorgevulde spuit
    • Netherlands (NL)
    • Luxembourg (LU)
    • Austria (AT)
    • France (FR)
    • Spain (ES)
    • Portugal (PT)
    • Italy (IT)
    • Sweden (SE)
    • Norway (NO)
    • Poland (PL)
      Rabipur
    • Hungary (HU)
      RABIPUR por és oldószer oldatos injekcióhoz előretöltött fecskendőben
    • Croatia (HR)
许可日期2016/03/17
最近更新日期2024/10/24
药物ATC编码
    • J07BG01 rabies, inactivated, whole virus
申请类型
  • TypeLevel1：Line Extension
  • TypeLevel2：Additional Strength/Form
  • TypeLevel3：Full Dossier Art 8.3(i) Dir 2001/83/EC
  • TypeLevel4：Biological: Vaccine
  • TypeLevel5：Prescription Only
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    市场状态Positive
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