欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号IE/H/1091/001
药品名称Meropenem 500 mg powder for solution for injection or infusion
活性成分
    • meropenem trihydrate 500.0 mg
剂型Powder for solution for infusion/injection
上市许可持有人Acino AG, (2168), (LOC-100038152), Leopoldstrasse 115, Schwabing-Freimann, Munich, Bavaria, 80804, Germany
参考成员国 - 产品名称Ireland (IE)
互认成员国 - 产品名称
    • United Kingdom (Northern Ireland) (XI)
      PL 17277/0207-0019
    • Poland (PL)
      Meropeetal
    • Greece (GR)
      PENEMNIA
    • Cyprus (CY)
许可日期2011/11/10
最近更新日期2024/03/14
药物ATC编码
    • J01DH02 meropenem
申请类型
  • TypeLevel1:[not specified]
  • TypeLevel2:[not specified]
  • TypeLevel3:[not specified]
  • TypeLevel4:[not specified]
  • TypeLevel5:[not specified]
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市场状态Positive
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