欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号SE/H/2305/001
药品名称Hydroxyzine Bluefish AB
活性成分
    • hydroxyzine hydrochloride 10.0 mg
剂型Film-coated tablet
上市许可持有人Bluefish Pharmaceuticals AB, Sweden
参考成员国 - 产品名称Sweden (SE)
Hydroxyzine Bluefish AB
互认成员国 - 产品名称
    • Austria (AT)
    • Poland (PL)
      Hydroxyzinum Bluefish
许可日期2023/11/27
最近更新日期2024/07/17
药物ATC编码
    • N05BB01 hydroxyzine
申请类型
  • TypeLevel1:Abridged
  • TypeLevel2:Initial Application
  • TypeLevel3:Generic Art 10.1 and 10.2 Dir 2001/83/EC
  • TypeLevel4:Chemical Substance
  • TypeLevel5:Prescription Only
附件文件下载
市场状态Positive
©2006-2024 Drugfuture->European Union HMA Authorisation of Medicines DataBase