欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号NL/V/0177/001
药品名称Euthanimal 20%
活性成分
    • PENTOBARBITAL 200.0 mg/ml
剂型Solution for injection
上市许可持有人Alfasan Nederland B.V. The Netherlands
参考成员国 - 产品名称Netherlands (NL)
Euthanimal 20%
互认成员国 - 产品名称
    • Germany (DE)
      Euthanimal 20%
    • Denmark (DK)
    • Belgium (BE)
      Euthanimal 20%
    • United Kingdom (Northern Ireland) (XI)
    • Ireland (IE)
      Euthanimal 20%
    • Spain (ES)
    • Portugal (PT)
    • Italy (IT)
    • Greece (GR)
    • Sweden (SE)
    • Finland (FI)
    • Poland (PL)
      Euthanimal 200 mg/ml, solution for injection
    • Latvia (LV)
      Euthanimal 20%
    • Lithuania (LT)
      EUTHANIMAL 20 %, 200 mg/ml, injekcinis tirpalas
    • Estonia (EE)
      Euthanimal 20%
    • Hungary (HU)
    • Bulgaria (BG)
    • Cyprus (CY)
    • Czechia (CZ)
    • Romania (RO)
    • Slovenia (SI)
    • Malta (MT)
许可日期2013/05/29
最近更新日期2025/05/20
药物ATC编码
    • QN51AA01 pentobarbital
申请类型
  • TypeLevel1：[not specified]
  • TypeLevel2：[not specified]
  • TypeLevel3：Full dossier - art 12.3 Dir 2001/82/EC
  • TypeLevel4：[not specified]
  • TypeLevel5：[not specified]
附件文件下载
市场状态Positive
©2006-2025 Drugfuture->European Union HMA Authorisation of Medicines DataBase