欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号CZ/H/0351/001
药品名称Vancomycin Mylan 500 mg, powder for solution for infusion
活性成分
    • Vancomycin hydrochloride 500.0 mg
剂型Powder for solution for infusion
上市许可持有人VIATRIS LIMITED Damastown Industrial Park, Mulhuddart Dublin 15 Ireland
参考成员国 - 产品名称Czechia (CZ)
Vancomycin Viatris
互认成员国 - 产品名称
    • Norway (NO)
    • Romania (RO)
    • Sweden (SE)
    • Croatia (HR)
    • Belgium (BE)
      Vancomycine Viatris 500 mg Powder for solution for infusion
    • Ireland (IE)
    • Italy (IT)
    • Greece (GR)
    • Cyprus (CY)
      VANCOMYCIN WELDING PHARMA FRANCE 500mg PWD FOR SOL FOR INFUSION
    • Slovakia (SK)
    • Slovenia (SI)
    • Denmark (DK)
    • Luxembourg (LU)
许可日期2011/04/19
最近更新日期2024/09/27
药物ATC编码
    • J01XA01 vancomycin
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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