欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号SI/H/0149/001
药品名称Moxifloxacin 400 mg film-coated tablets
活性成分
    • Moxifloxacin hydrochloride 455.0 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Slovenia (SI)
Moloxin 400 mg filmsko obložene tablete
互认成员国 - 产品名称
    • Germany (DE)
      Moxifloxacin TAD 400 mg Filmtabletten
    • Denmark (DK)
    • Austria (AT)
      Moxifloxacin Krka 400 mg Filmtabletten
    • France (FR)
    • Spain (ES)
    • Portugal (PT)
    • Italy (IT)
    • Sweden (SE)
    • Finland (FI)
    • Poland (PL)
      Moloxin
    • Lithuania (LT)
      Moflaxa 400 mg plėvele dengtos tabletės
    • Estonia (EE)
      MOFLAXA
    • Hungary (HU)
      MOXIBIOT 400 mg filmtabletta
    • Bulgaria (BG)
      Moloxin
    • Romania (RO)
      Moloxin 400 mg comprimate filmate
    • Slovakia (SK)
      Moloxin 400mg filmom obalené tablety
    • Croatia (HR)
许可日期2014/04/11
最近更新日期2025/02/07
药物ATC编码
    • J01MA14 moxifloxacin
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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