欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号SE/H/0153/001
药品名称Pentavac
活性成分
    • diphtheria toxoid, adsorbed 30.0 IU
    • Haemagglutinin Isolated From Er1k A Equi Brentwood 79 25.0 µg
    • haemophilus influenzae type b (strain PBCC 197) capsular oligosaccharide conjugated to diphtheria CMR197 protein 10.0 µg
    • Pertussis toxoid 25.0 µg
    • Polio virus type 1, inactivated 40.0 IU
    • Polio virus type 1, inactivated 32.0 IU
    • Polio virus type 2, inactivated 8.0 IU
    • tetanus toxoid, adsorbed 40.0 IU
剂型Powder and suspension for suspension for injection
上市许可持有人Sanofi Pasteur Europe, France
参考成员国 - 产品名称Sweden (SE)
Pentavac
互认成员国 - 产品名称
    • Iceland (IS)
    • Denmark (DK)
    • Belgium (BE)
    • Luxembourg (LU)
    • Portugal (PT)
      Pentavac
    • Greece (GR)
    • Finland (FI)
许可日期1998/08/03
最近更新日期2025/02/10
药物ATC编码
    • J07CA06 diphtheria-haemophilus influenzae B-pertussis-poliomyelitis-tetanus
申请类型
  • TypeLevel1:[not specified]
  • TypeLevel2:[not specified]
  • TypeLevel3:Full Dossier Article 4.8 Di 65/65
  • TypeLevel4:[not specified]
  • TypeLevel5:[not specified]
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市场状态Positive
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