欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号IE/V/0359/001
药品名称Bioestrovet
活性成分
    • cloprostenol 0.25 mg/ml
剂型Solution for injection
上市许可持有人Vetoquinol Ireland Limited, First Floor, Segrave House, 19/20 Earlsfort Terrace, Dublin 2, Ireland
参考成员国 - 产品名称Ireland (IE)
Bioestrovet 0.250 mg/ml solution for injection for cattle
互认成员国 - 产品名称
    • Spain (ES)
    • Portugal (PT)
    • Italy (IT)
    • Greece (GR)
    • Poland (PL)
    • Latvia (LV)
    • Lithuania (LT)
    • Estonia (EE)
      Bioestrovet
    • Hungary (HU)
    • Bulgaria (BG)
    • Cyprus (CY)
    • Romania (RO)
    • Slovenia (SI)
    • Malta (MT)
    • Croatia (HR)
    • Czechia (CZ)
      Bioestrovet 0,250 mg/ml injekční roztok pro skot
    • Slovakia (SK)
    • United Kingdom (Northern Ireland) (XI)
    • Germany (DE)
    • Denmark (DK)
    • Belgium (BE)
    • Netherlands (NL)
    • Luxembourg (LU)
    • Austria (AT)
    • France (FR)
      BIOESTROVET 0,250 MG/ML SOLUTION INJECTABLE POUR BOVINS (14319)
许可日期2016/12/21
最近更新日期2023/09/14
药物ATC编码
    • QG02AD90 cloprostenol
申请类型
  • TypeLevel1：[not specified]
  • TypeLevel2：[not specified]
  • TypeLevel3：Generic - art 13.2 Dir 2001/82/EC
  • TypeLevel4：[not specified]
  • TypeLevel5：[not specified]
附件文件下载
市场状态Positive
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