欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号DE/V/0212/001
药品名称Nobilis RT+IBmulti+G+ND
活性成分
    • ARTV strain BUT#8544 ind > 9,5log2 ELISA units 0.0 [no unit]
    • ARTV strain BUT#8544; IBDV strain D78; IBV strain 249g; IBV stra 0.0 [no unit]
    • IBDV strain D78 ind >14,5log2 VN units 0.0 [no unit]
    • IBV strain 249g ind > 4,0log2 VN units 0.0 [no unit]
    • IBV strain M41 ind >4,0log2 VN units 0.0 [no unit]
剂型Emulsion for injection
上市许可持有人Intervet International B.V. Wim de Korverstraat 35 5831 AN Boxmeer The Netherlands
参考成员国 - 产品名称Germany (DE)
互认成员国 - 产品名称
    • Belgium (BE)
    • Netherlands (NL)
    • Luxembourg (LU)
    • United Kingdom (Northern Ireland) (XI)
    • Ireland (IE)
    • Austria (AT)
    • France (FR)
      NOBILIS RT REPRO
    • Spain (ES)
    • Portugal (PT)
    • Italy (IT)
    • Greece (GR)
    • Denmark (DK)
许可日期2000/05/27
最近更新日期2025/06/13
药物ATC编码
    • QI01AA06 avian infectious bronchitis virus + avian infectious bursal (gumboro) disease virus + newcastle disease virus / paramyxovirus + avian rhinotracheitis virus
    • QI01AA Inactivated viral vaccines
申请类型
  • TypeLevel1：[not specified]
  • TypeLevel2：[not specified]
  • TypeLevel3：Full Dossier (art.5)
  • TypeLevel4：[not specified]
  • TypeLevel5：[not specified]
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市场状态Positive
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