欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/6067/001
药品名称Difterie-, Tetanus,- Poliomyelitisvaccine
活性成分
    • diphtheria toxoid, adsorbed 5.0 IU/ml
    • Polio virus type 1, inactivated 40.0 DAgU/ml
    • Polio virus type 2, inactivated 4.0 DAgU/ml
    • Polio virus type 3, inactivated 7.5 DAgU/ml
    • tetanus toxoid, adsorbed 20.0 IU/ml
剂型Suspension for injection
上市许可持有人Bilthoven Biologicals B.V. Antonie van Leeuwenhoeklaan 9 3721 MA, Bilthoven The Netherlands
参考成员国 - 产品名称Netherlands (NL)
Difterie-, Tetanus-, Poliomyelitisvaccin, suspensie voor injectie
互认成员国 - 产品名称
    • Malta (MT)
许可日期2024/01/22
最近更新日期2024/12/30
药物ATC编码
    • J07CA01 diphtheria-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:Biological: Vaccine
  • TypeLevel5:Prescription Only
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市场状态Positive
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