欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号FR/V/0262/001
药品名称Anaestamine 100 mg/ml solution for injection
活性成分
    • ketamine hydrochloride 100.0 mg
剂型Solution for injection
上市许可持有人Le Vet Beheer B.V
参考成员国 - 产品名称France (FR)
ANAESTAMINE (13630)
互认成员国 - 产品名称
    • Denmark (DK)
    • Belgium (BE)
      Anaestamine 100 mg/ml
    • Netherlands (NL)
    • Luxembourg (LU)
    • Iceland (IS)
      Aniketam vet. 100 mg/ml Stungulyf
    • United Kingdom (Northern Ireland) (XI)
    • Ireland (IE)
      Anaestamine 100mg/ml Solution for injection
    • Austria (AT)
      Anaestamine 100 mg/ml Injektionslösung für Tiere
    • Spain (ES)
    • Portugal (PT)
    • Italy (IT)
    • Greece (GR)
    • Sweden (SE)
    • Norway (NO)
    • Finland (FI)
    • Poland (PL)
    • Latvia (LV)
    • Lithuania (LT)
    • Estonia (EE)
      Aniketam
    • Hungary (HU)
    • Czechia (CZ)
      Anaestamine 100 mg/ml injekční roztok
    • Romania (RO)
    • Slovakia (SK)
许可日期2014/06/18
最近更新日期2019/10/29
药物ATC编码
    • QN01AX03 ketamine
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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