欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号DE/H/1588/001
药品名称MOXIFLOXACIN ALCON 5 mg/ml Augentropfen
活性成分
    • moxifloxacin hydrochloride 5.45 mg/ml
剂型Eye drops, solution
上市许可持有人Novartis Pharma GmbH Roonstr. 25 90429 Nürnberg Germany
参考成员国 - 产品名称Germany (DE)
2172577
互认成员国 - 产品名称
    • Finland (FI)
    • Greece (GR)
    • Italy (IT)
    • Portugal (PT)
    • Iceland (IS)
      flaska með DROP Vigamox 5 mg/ml Augndropar, lausn
    • Luxembourg (LU)
    • Netherlands (NL)
    • Belgium (BE)
    • Denmark (DK)
    • Hungary (HU)
      VIGAMOX 5 mg/ml oldatos szemcsepp
    • Lithuania (LT)
      VIGAMOX 5mg/ml akių lašai (tirpalas)
    • Sweden (SE)
    • Malta (MT)
    • Slovenia (SI)
    • Slovakia (SK)
    • Romania (RO)
      Vigamox 5mg/ml, picături oftalmice soluţie
    • Czechia (CZ)
    • Cyprus (CY)
    • Bulgaria (BG)
      Vigamox
    • Estonia (EE)
    • Latvia (LV)
    • Poland (PL)
      Vigamox
    • Spain (ES)
许可日期2009/05/05
最近更新日期2024/04/17
药物ATC编码
    • S01AE07 moxifloxacin
申请类型
  • TypeLevel1:Known Active Substance
  • TypeLevel2:Initial Application
  • TypeLevel3:Full Dossier Art 8.3(i) Dir 2001/83/EC
  • TypeLevel4:Chemical Substance
  • TypeLevel5:Prescription Only
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市场状态Positive
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