欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号DE/V/0021/001
药品名称Rispoval IBR-Marker inactivatum
活性成分
    • bovine herpesvirus inactivated 2.0 ml
剂型Suspension for injection
上市许可持有人Zoetis Deutschland GmbH Schellingstr. 1 10785 Berlin
参考成员国 - 产品名称Germany (DE)
互认成员国 - 产品名称
    • Belgium (BE)
      Rispoval IBR-Marker inactivatum
    • Netherlands (NL)
      Bayovac IBR-Marker inactivatum
    • Luxembourg (LU)
      Bayovac IBR-Marker inactivatum
    • United Kingdom (Northern Ireland) (XI)
      Bayovac IBR-Marker inactivatum
    • Ireland (IE)
      Bayovac IBR-Marker inactivatum
    • Spain (ES)
      Bayovac IBR-Marker inactivatum
    • Italy (IT)
      Bayovac IBR-Marker inactivatum
    • Portugal (PT)
    • Poland (PL)
    • Latvia (LV)
      Rispoval IBR-Marker Vivum
    • Lithuania (LT)
    • Estonia (EE)
    • Hungary (HU)
    • Czechia (CZ)
    • Romania (RO)
    • Slovakia (SK)
    • Slovenia (SI)
    • Malta (MT)
许可日期2008/04/05
最近更新日期2024/09/24
药物ATC编码
    • QI02A CATTLE
    • QI02 IMMUNOLOGICALS FOR BOVIDAE
    • QI IMMUNOLOGICALS
    • QI02AA03 bovine rhinotracheitis virus (IBR)
    • QI02AA 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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