欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/0585/002
药品名称Terbinafine 250, tablets 250 mg
活性成分
    • terbinafine 250.0 mg
剂型Tablet
上市许可持有人Stichting Registratie Beheer Bosstraat 69 3766 AC SOEST The Netherlands
参考成员国 - 产品名称Netherlands (NL)
互认成员国 - 产品名称
    • Belgium (BE)
    • Luxembourg (LU)
    • Poland (PL)
    • Latvia (LV)
      Terbinafīns Sandoz 250mg tabletes
    • Lithuania (LT)
      Terbinafine Sandoz 250mg tabletės
    • Estonia (EE)
      TERBINAFINE SANDOZ 250 MG TABLETID
    • Hungary (HU)
      Tefine 250mg tabletta
    • Slovakia (SK)
      Tefine 250 mg tablety
    • Slovenia (SI)
      Tefine 250 mg tablete
许可日期2005/04/20
最近更新日期2020/03/17
药物ATC编码
    • D01BA02 terbinafine
申请类型
  • TypeLevel1:Abridged
  • TypeLevel2:Additional Strength/Form
  • TypeLevel3:Generic [Article 10.1.(a)(iii), first paragraph]
  • TypeLevel4:Chemical Substance
  • TypeLevel5:Prescription Only
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    市场状态Positive
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