欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号DK/H/2042/004
药品名称Ropinirol “Actavis”
活性成分
    • ropinirole 6.0 mg
剂型Prolonged-release tablet
上市许可持有人splitting: New splitted procedure number is UK/H/6896/001 and PT/H/2115/001 Actavis Group PTC ehf. Dalshraun 1, 220 Hafnarfjörður Iceland
参考成员国 - 产品名称Denmark (DK)
Ropinirol "Actavis"
互认成员国 - 产品名称
    许可日期2012/03/14
    最近更新日期2024/01/08
    药物ATC编码
      • N04BC04 ropinirole
    申请类型
    • TypeLevel1:Abridged
    • TypeLevel2:Additional Strength/Form
    • TypeLevel3:Other Generic application Art 10.3 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