欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/0630/002
药品名称Sumatriptan 100 mg
活性成分
    • sumatriptan 100.0 mg
剂型Tablet
上市许可持有人Pilot: Merging: Procedure was merged with Procedure NL/H/0629/002 (on 31 March 2017) Hexal AG Industiestrase 25 83607 Holzkirchen Germany
参考成员国 - 产品名称Netherlands (NL)
互认成员国 - 产品名称
    许可日期2005/10/10
    最近更新日期2017/04/04
    药物ATC编码
      • N02CC01 sumatriptan
    申请类型
    • TypeLevel1:Abridged
    • TypeLevel2:Additional Strength/Form
    • TypeLevel3:Generic [Article 10.1.(a)(iii), first paragraph]
    • TypeLevel4:Chemical Substance
    • TypeLevel5:Prescription Only
    附件文件下载
    市场状态Withdrawn(注:已撤市)
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