欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号DE/H/0155/001
药品名称Avalox 400 mg Filmtabletten
活性成分
    • moxifloxacin hydrochloride 437.0 mg
剂型Film-coated tablet
上市许可持有人Bayer Vital GmbH Kaiser-Wilhelm-Allee 70 51373 Leverkusen Germany
参考成员国 - 产品名称Germany (DE)
互认成员国 - 产品名称
    • Bulgaria (BG)
    • Denmark (DK)
    • Belgium (BE)
    • Luxembourg (LU)
      Avelox
    • Austria (AT)
      Avelox 400 mg Filmtabletten
    • France (FR)
    • Portugal (PT)
    • Italy (IT)
    • Greece (GR)
    • Sweden (SE)
    • Finland (FI)
    • Latvia (LV)
      Avelox 400 mg Tablets
    • Lithuania (LT)
      Avelox 400 mg plėvele dengtos tabletės
    • Estonia (EE)
      AVELOX
    • Romania (RO)
      Avelox 400 mg Comprimate filmate
    • Cyprus (CY)
      Avelox 400 mg Tablets
    • Czechia (CZ)
许可日期1999/10/08
最近更新日期2024/06/13
药物ATC编码
    • J01MA14 moxifloxacin
申请类型
  • TypeLevel1:[not specified]
  • TypeLevel2:[not specified]
  • TypeLevel3:Full Dossier Article 4.8 Di 65/65
  • TypeLevel4:[not specified]
  • TypeLevel5:[not specified]
附件文件下载
市场状态Positive
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