欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号NL/H/3289/001
药品名称Pemetrexed SUN 100 mg powder for concentrate for solution for infusion
活性成分
    • Pemetrexed disodium 100.0 mg
剂型Powder for concentrate for solution for infusion
上市许可持有人Sun Pharmaceutical Industries Europe B.V. Polarisavenue 87, Hoofddorp 2132 JH The Netherlands
参考成员国 - 产品名称Netherlands (NL)
Pemetrexed SUN 100 mg poeder voor concentraat voor oplossing voor infusie
互认成员国 - 产品名称
    • United Kingdom (Northern Ireland) (XI)
    • Spain (ES)
    • Italy (IT)
    • Poland (PL)
      Pemetreksed SUN
    • Romania (RO)
      Pemetrexed SUN 100 mg pulbere pentru concentrat pentru soluţie perfuzabilă
许可日期2016/01/20
最近更新日期2025/07/10
药物ATC编码
    • L01BA04 pemetrexed
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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