欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号FI/H/0668/001
药品名称Fexofenadin Sandoz 120 mg
活性成分
    • fexofenadine hydrochloride 120.0 mg
剂型Film-coated tablet
上市许可持有人NEW RMS DE/H/2632/01 Sandoz A/S C.F. Tietgens Boulevard 40 5220 Odense SØ DENMARK
参考成员国 - 产品名称Finland (FI)
互认成员国 - 产品名称
    • Germany (DE)
      Fexofenadin - Sandoz 120 mg Filmtabletten
    • Denmark (DK)
      Fexofenadin "Sandoz"
    • Netherlands (NL)
    • United Kingdom (Northern Ireland) (XI)
    • Italy (IT)
    • Sweden (SE)
      Fexofenadin Sandoz
    • Hungary (HU)
      Fexofenadin-Sandoz 120 mg ftabl.
    • Slovakia (SK)
      Fexofenadin Sandoz 120 mg filmom obalené tablety
    • Slovenia (SI)
      Feksofenadin Lek 120 mg filmsko obložene tablete
许可日期2008/07/16
最近更新日期2012/01/09
药物ATC编码
    • R06AX26 fexofenadine
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
附件文件下载
    市场状态Positive
    ©2006-2024 Drugfuture->European Union HMA Authorisation of Medicines DataBase