欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号AT/H/0366/001
药品名称Moxifloxacin Sandoz 400 mg -Filmtabletten
活性成分
    • Moxifloxacin hydrochloride 400.0 mg
剂型Film-coated tablet
上市许可持有人Sandoz GmbH Biochemiestrasse 10 A-6250 Kundl
参考成员国 - 产品名称Austria (AT)
Moxifloxacin Sandoz 400 mg - Filmtabletten
互认成员国 - 产品名称
    • Netherlands (NL)
      Moxifloxacine Sandox 400 mg, filmomhulde tabletten
    • Greece (GR)
      MOXIFLOXACIN/SANDOZ
    • Latvia (LV)
      Moxifloxacin Sandoz 400 mg apvalkotās tabletes
    • Lithuania (LT)
      Moxifloxacin Sandoz 400 mg plėvele dengtos tabletės
    • Belgium (BE)
    • France (FR)
    • Spain (ES)
    • Bulgaria (BG)
      Cimocinox
许可日期2011/04/11
最近更新日期2024/12/09
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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