欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号EE/H/0103/002
药品名称Levofloxacin Actavis
活性成分
    • levofloxacin hemihydrate 500.0 mg
剂型Film-coated tablet
上市许可持有人Actavis Group PTC ehf. Reykjavikurvegur 76-78 220 Hafnarfjördur Iceland
参考成员国 - 产品名称Estonia (EE)
LEVOFLOXACIN ACTAVIS
互认成员国 - 产品名称
    • Malta (MT)
      Levoxa
    • Iceland (IS)
    • Portugal (PT)
    • Poland (PL)
    • Hungary (HU)
      Levoxa 500 mg filmtabletta
    • Romania (RO)
      Levofloxacină Actavis 500 mg comprimate filmate
许可日期2007/12/27
最近更新日期2012/10/08
药物ATC编码
    • J01MA12 levofloxacin
申请类型
  • TypeLevel1:Abridged
  • TypeLevel2:Additional Strength/Form
  • 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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