欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号IE/V/0514/005
药品名称Vetoryl 5 mg hard capsules for dogs
活性成分
    • trilostane 5.0 mg
剂型Capsule, hard
上市许可持有人Dechra Regulatory B.V. Handelsweg 25 5531 AE Bladel Netherlands
参考成员国 - 产品名称Ireland (IE)
互认成员国 - 产品名称
    • Germany (DE)
    • Denmark (DK)
      Vetoryl
    • Belgium (BE)
      Vetoryl 5 mg
    • Netherlands (NL)
    • Luxembourg (LU)
    • United Kingdom (Northern Ireland) (XI)
    • Austria (AT)
    • France (FR)
    • Spain (ES)
    • Portugal (PT)
    • Italy (IT)
    • Greece (GR)
    • Sweden (SE)
    • Norway (NO)
    • Finland (FI)
    • Poland (PL)
    • Hungary (HU)
    • Czechia (CZ)
    • Slovakia (SK)
    • Slovenia (SI)
    • Croatia (HR)
许可日期2020/11/18
最近更新日期2024/08/23
药物ATC编码
    • QH02CA01 trilostane
申请类型
  • TypeLevel1:non-food
  • TypeLevel2:Pharmaceutical
  • 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
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