欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号DE/H/0145/001
药品名称Infanrix-IPV+Hib (DTPa-IPV+Hib)
活性成分
    • Diphteria toxoid (DT) 30.0 IU
    • Filamentous haemagglutinin (FHA) 25.0 µg
    • Hib PRP covalently bound to TT (30µg) 10.0 µg
    • Inactivated Polio Virus Type I 40.0 DU
    • Inactivated Polio Virus Type II 8.0 DU
    • Inactivated Polio Virus Type III 32.0 DU
    • pertactin 8.0 µg
    • Pertussis toxoid (PT) 25.0 µg
    • Pertussis toxoid (PT), Filamentous haemagglutinin (FHA), Pertact 0.0 [no unit]
    • Tetanus toxoid (TT) 40.0 IU
剂型Suspension for injection
上市许可持有人GlaxoSmithKline GmbH & Co. KG Theresienhöhe 11 D-80339 München
参考成员国 - 产品名称Germany (DE)
互认成员国 - 产品名称
    • Czechia (CZ)
      Infarix TM – IPV Hib
    • Slovakia (SK)
    • United Kingdom (Northern Ireland) (XI)
    • Ireland (IE)
      Infanrix-IPV+Hib
    • Portugal (PT)
      Infanrix-IPV+Hib
    • Greece (GR)
      Infanrix-IPV+Hib
    • Finland (FI)
      Infanrix-IPV+Hib
许可日期1998/12/17
最近更新日期2016/10/13
药物ATC编码
    • J07CA06 diphtheria-haemophilus influenzae B-pertussis-poliomyelitis-tetanus
申请类型
  • TypeLevel1:New Active Substance
  • TypeLevel2:Initial Application
  • TypeLevel3:Full Dossier Article 4.8 Di 65/65
  • TypeLevel4:Biological: Vaccine
  • TypeLevel5:Prescription Only
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