欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号NL/H/4114/002
药品名称Pemetrexed 500 mg powder for concentrate for solution for infusion
活性成分
    • pemetrexed disodium 500.0 mg
剂型Powder for concentrate for solution for infusion
上市许可持有人Waverley Pharma Europe Limited Alexandra House, Office# 234, The Sweepstakes, Dublin 4 D04 C7H2 Ireland
参考成员国 - 产品名称Netherlands (NL)
Pemetrexed 500 mg poeder voor concentraat voor oplossing voor infusie
互认成员国 - 产品名称
    • Luxembourg (LU)
    • United Kingdom (Northern Ireland) (XI)
    • Spain (ES)
    • Poland (PL)
      Pemetrexed Waverly
    • Czechia (CZ)
      Pemetrexed powder for concentrate for solution for infusion
    • Slovenia (SI)
许可日期2019/11/28
最近更新日期2024/02/21
药物ATC编码
    • L01BA04 pemetrexed
申请类型
  • TypeLevel1：Abridged
  • TypeLevel2：Additional Strength/Form
  • 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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