欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号HR/H/0100/001
药品名称Levalox 250 mg filmom obložene tablete
活性成分
    • levofloxacin hemihydrate 256.23 mg
剂型Film-coated tablet
上市许可持有人Krka d.d. Novo Mesto Šmarješka cesta 6, 8501 Novo Mesto Slovenia
参考成员国 - 产品名称Croatia (HR)
Levalox 250 mg filmom obložene tablete
互认成员国 - 产品名称
    • Ireland (IE)
    • Austria (AT)
      Levofloxacin Krka 250 mg Filmtabletten
    • Sweden (SE)
    • Finland (FI)
    • Poland (PL)
    • Latvia (LV)
      Levalox 250 mg apvalkotās tabletes
    • Lithuania (LT)
      Levalox 250 mg plėvele dengtos tabletės
    • Estonia (EE)
      LEVNIBIOT
    • Hungary (HU)
      LEVNIBIOT 250 mg filmtabletta
    • Romania (RO)
      LEVALOX 250 mg comprimate filmate
    • Slovakia (SK)
    • Slovenia (SI)
    • Italy (IT)
许可日期2015/01/27
最近更新日期2024/10/17
药物ATC编码
    • J01MA12 levofloxacin
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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