欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号FI/H/0779/001
药品名称Tramadol Vitabalans 50 mg
活性成分
    • Tramadol hydrochloride 50.0 mg
剂型Tablet
上市许可持有人Vitabalans Oy Varastokatu 8 13500 Hämeenlinna FINLAND
参考成员国 - 产品名称Finland (FI)
Tramadol Vitabalans 50 mg tabletti
互认成员国 - 产品名称
    • Denmark (DK)
      Tramadol "Vitabalans"
    • Sweden (SE)
    • Norway (NO)
      Tramadol Vitabalans
    • Poland (PL)
      Tramadol Vitabalans
    • Latvia (LV)
      Tramadol Vitabalans 50 mg tabletes
    • Lithuania (LT)
      Tramadol Vitabalans 50 mg tabletės
    • Estonia (EE)
      TRAMADOL VITABALANS
    • Hungary (HU)
      TRAMADOL VITABALANS 50 mg tabletta
    • Czechia (CZ)
      Tramadol Vitabalans 50 mg tablety
    • Slovakia (SK)
      Tramadol Vitabalans 50 mg tablety
    • Slovenia (SI)
许可日期2012/07/26
最近更新日期2024/09/26
药物ATC编码
    • N02AX02 tramadol
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
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    市场状态Positive
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