欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号UK/H/5562/007
药品名称Pramipexole Mylan 3.15 mg Prolonged-release Tablets
活性成分
    • PRAMIPEXOLE DIHYDROCHLORIDE monohydrate 3.15 mg
剂型Prolonged-release tablet
上市许可持有人Generics UK Albany Gate, Darkes Lane, Potters Bar, Herts EN6 1 AG
参考成员国 - 产品名称United Kingdom (UK)
Pramipexole Mylan 3.15 mg Prolonged-release Tablets
互认成员国 - 产品名称
    • Belgium (BE)
    • Austria (AT)
    • Germany (DE)
      Pramipexol Mylan 3,15 mg Retardtablette
    • Luxembourg (LU)
    • Netherlands (NL)
    • Cyprus (CY)
    • Greece (EL)
      PRAMIPEXOLE/GENERICS
    • Italy (IT)
许可日期2015/03/30
最近更新日期2015/05/22
药物ATC编码
    • N04BC05 pramipexole
申请类型
  • TypeLevel1：Abridged
  • TypeLevel2：Additional Strength/Form
  • TypeLevel3：Generic
  • TypeLevel4：Chemical Substance
  • TypeLevel5：Prescription Only
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