欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号DK/V/0107/001
药品名称Porcilis Glässer Vet.
活性成分
    • Inactivated Haemophilus parasuis strain 4800 0.0 [no unit]
剂型Suspension for injection
上市许可持有人Intervet International BV Wim de Korverstraat 35 NL - 5831 AN Boxmeer the Netherlands
参考成员国 - 产品名称Denmark (DK)
互认成员国 - 产品名称
    • Belgium (BE)
      Porcilis Glässer
    • Luxembourg (LU)
    • Austria (AT)
    • Slovakia (SK)
    • Czechia (CZ)
    • Cyprus (CY)
    • Hungary (HU)
    • Estonia (EE)
    • Latvia (LV)
    • Poland (PL)
      Porcilis Glasser
    • Finland (FI)
    • Norway (NO)
    • Greece (GR)
    • Italy (IT)
    • Portugal (PT)
    • Spain (ES)
    • France (FR)
      PORCILIS GLASSER
    • Ireland (IE)
    • United Kingdom (Northern Ireland) (XI)
    • Netherlands (NL)
    • Germany (DE)
      Porcilis Glässer
许可日期2003/12/23
最近更新日期2024/09/26
药物ATC编码
    • QI09AB07 actinobacillus/haemophilus vaccine
申请类型
  • TypeLevel1：[not specified]
  • TypeLevel2：[not specified]
  • TypeLevel3：Full Dossier (art.5)
  • TypeLevel4：[not specified]
  • TypeLevel5：[not specified]
附件文件下载
市场状态Positive
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