欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号AT/H/0314/003
药品名称Pramipexol Viatris 0,35 mg Tabletten
活性成分
    • Pramipexole 0.35 mg
剂型Tablet
上市许可持有人Viatris Limited Damastown Industrial Park, Mulhuddart, Dublin 15, DUBLIN, Irland
参考成员国 - 产品名称Austria (AT)
Pramipexol Viatris 0,35 mg Tabletten
互认成员国 - 产品名称
    • Denmark (DK)
      Pramipexole "Mylan"
    • Belgium (BE)
      Pramipexole Viatris 0.35 mg tablet
    • Netherlands (NL)
    • United Kingdom (Northern Ireland) (XI)
许可日期2010/07/15
最近更新日期2025/01/07
药物ATC编码
    • N04BC05 pramipexole
申请类型
  • TypeLevel1:Abridged
  • TypeLevel2:Additional Strength/Form
  • 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
©2006-2025 Drugfuture->European Union HMA Authorisation of Medicines DataBase