欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号NL/H/4660/001
药品名称Sumatriptan SUN 3 mg/0,5 ml Solution for injection in pre-filled pen
活性成分
    • Sumatriptan succinate 6.0 mg/ml
剂型Solution for injection
上市许可持有人Sun Pharmaceutical Industries Europe B.V. Polarisavenue 87 2132 JH Hoofddorp Netherlands
参考成员国 - 产品名称Netherlands (NL)
Sumatriptan SUN 3 mg/0,5 ml oplossing voor injectie in voorgevulde pen
互认成员国 - 产品名称
    • Germany (DE)
      MIGRAPEN 3 mg/0,5 ml Injektionslösung im Fertigpen
    • United Kingdom (Northern Ireland) (XI)
    • France (FR)
    • Spain (ES)
    • Italy (IT)
    • Sweden (SE)
    • Norway (NO)
      Sumatriptan SUN
    • Poland (PL)
      Sumatriptan SUN
    • Romania (RO)
      Sumatriptan SUN 3 mg/0,5 ml soluție injectabilă
许可日期2020/02/12
最近更新日期2025/10/08
药物ATC编码
    • N02CC01 sumatriptan
申请类型
  • TypeLevel1：Abridged
  • TypeLevel2：Initial Application
  • TypeLevel3：Other
  • TypeLevel4：Chemical Substance
  • TypeLevel5：Prescription Only
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市场状态Positive
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