欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号HU/H/0406/001
药品名称TETRAXIM
活性成分
    • diphtheria toxoid, adsorbed 30.0 IU
    • Pertussis toxoid 25.0 µg
    • POLIOMYELITIS VACCINE 40.0 DU
    • Tetanus toxoid 40.0 IU
剂型SUSPENSION FOR INJECTION IN PRE-FILLED SYRINGE
上市许可持有人Sanofi Pasteur SA 2 avenue Pont Pasteur Lyon 69007 France
参考成员国 - 产品名称Hungary (HU)
TETRAXIM szuszpenziós injekció előretöltött fecskendőben
互认成员国 - 产品名称
    • Spain (ES)
    • Poland (PL)
      Tetraxim
    • Cyprus (CY)
      TETRAXIM
    • Czechia (CZ)
      TETRAXIM
    • Slovakia (SK)
      TETRAXIM
    • Croatia (HR)
      Tetraxim, suspenzija za injekciju u napunjenoj štrcaljki, cjepivo protiv difterije, tetanusa, hripavca (nestanično, komponentno) i poliomijelitisa (inaktivirano), adsorbirano
许可日期2016/04/21
最近更新日期2024/10/28
药物ATC编码
    • J07CA02 diphtheria-pertussis-poliomyelitis-tetanus
申请类型
  • TypeLevel1:Known Active Substance
  • TypeLevel2:Initial Application
  • TypeLevel3:Full Dossier Art 8.3(i) Dir 2001/83/EC
  • TypeLevel4:Chemical Substance
  • TypeLevel5:Prescription Only
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市场状态Positive
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