欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/0675/001
药品名称Sumatriptan Merck 50 mg, filmcoated tablets
活性成分
    • sumatriptan 50.0 mg
剂型Film-coated tablet
上市许可持有人Merck Genercs B.V. Dieselweg 25 3752 LB Bunschoten, The Netherlands
参考成员国 - 产品名称Netherlands (NL)
Sumatriptan Mylan 50 mg
互认成员国 - 产品名称
    • Denmark (DK)
    • Belgium (BE)
      Sumatriptan Viatris 50 mg filmomhulde tabletten
    • Sweden (SE)
    • Czechia (CZ)
许可日期2005/12/20
最近更新日期2024/02/14
药物ATC编码
    • N02CC01 sumatriptan
申请类型
  • TypeLevel1:Abridged
  • TypeLevel2:Initial Application
  • TypeLevel3:Generic [Article 10.1.(a)(iii), first paragraph]
  • TypeLevel4:Chemical Substance
  • TypeLevel5:Prescription Only
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市场状态Positive
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