欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号FI/H/0751/001
药品名称Fluoxetine Vitabalans 20 mg
活性成分
    • fluoxetine hydrochloride 22.36 mg
剂型Film-coated 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)
Fluoxetine Vitabalans
互认成员国 - 产品名称
    • Sweden (SE)
    • Iceland (IS)
    • Czechia (CZ)
      FLUOZACTIN 20 mg potahované tablety
    • Germany (DE)
      FLUOZACTIN 20 mg Filmtabletten
    • Denmark (DK)
    • Estonia (EE)
      FLUOXETINE VITABALANS
    • Hungary (HU)
      FLUOXETINE VITABALANS 20 mg filmtabletta
    • Lithuania (LT)
      Fluoxetine Vitabalans 20 mg plėvele dengtos tabletės
    • Latvia (LV)
      Fluoxetine Vitabalans 20 mg apvalkotās tabletes
    • Norway (NO)
    • Poland (PL)
      Fluoxetine Vitabalans
    • Slovenia (SI)
      Fluoksetin Vitabalans 20 mg filmsko obložene tablete
    • Slovakia (SK)
      FLUOZACTIN
许可日期2011/03/23
最近更新日期2021/11/12
药物ATC编码
    • N06AB03 fluoxetine
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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