欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号DK/H/0143/002
药品名称diTekiBooster
活性成分
    • diphtheria toxoid, adsorbed 2.0 IU
    • pertussis toxoid 20.0 µg
    • tetanus toxoid, adsorbed 20.0 IU
剂型SUSPENSION FOR INJECTION IN PRE-FILLED SYRINGE
上市许可持有人AJ Vaccines A/S Artillerivej 5 2300 København S Denmark
参考成员国 - 产品名称Denmark (DK)
diTekiBooster
互认成员国 - 产品名称
    • Germany (DE)
      Tdap-IMMUN
    • Belgium (BE)
      BoosterTdaP 0.5ml Suspension for injection in pre-filled syringe
    • Netherlands (NL)
    • Iceland (IS)
      TdaPBooster 0,5 ml Stungulyf, dreifa í áfylltri sprautu
    • Ireland (IE)
    • Austria (AT)
      dTaP Booster SSI Injektionssuspension in einer Fertigspritze
    • Italy (IT)
    • Sweden (SE)
    • Norway (NO)
    • Finland (FI)
    • Poland (PL)
      Tdap Szczepionka SSI
许可日期2013/04/24
最近更新日期2023/05/11
药物ATC编码
    • J07AJ52 pertussis, purified antigen, combinations with toxoids
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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