欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号ES/H/0101/002
药品名称Ketesse 25 mg
活性成分
    • Dexketoprofen 25.0 %
剂型Film-coated tablet
上市许可持有人Menarini, S.A.
参考成员国 - 产品名称Spain (ES)
互认成员国 - 产品名称
    • Germany (DE)
      Sympal 25 mg
    • Belgium (BE)
      KETESSE 25 mg tablets
    • Netherlands (NL)
      KETESSE 25 mg tablets
    • Luxembourg (LU)
      Ketesse
    • United Kingdom (Northern Ireland) (XI)
      KETESSE 25 mg tablets
    • Ireland (IE)
      KETESSE 25 mg tablets
    • Austria (AT)
      Ketesse 25 mg - Filmtabletten
    • France (FR)
      KETESSE 25 mg tablets
    • Portugal (PT)
      KETESSE 25 mg tablets
    • Italy (IT)
      KETESSE 25 mg tablets
    • Greece (GR)
      KETESSE 25 mg tablets
    • Finland (FI)
      KETESSE 25 mg tablets
    • Poland (PL)
      Dexak
    • Latvia (LV)
      Dolmen 25 mg film-coated tablets
    • Lithuania (LT)
      Dolmen 25 mg plėvele dengtos tabletės
    • Estonia (EE)
      DOLMEN
    • Hungary (HU)
      Enantyum és Ketesse
    • Cyprus (CY)
      ENANTYUM F.C. TABLETS 25MG
    • Czechia (CZ)
      DEXOKET 25 mg Tablety
    • Slovakia (SK)
      Ketesse 25 mg tbl 2106/0754
    • Slovenia (SI)
    • Malta (MT)
许可日期1997/12/03
最近更新日期2025/02/14
药物ATC编码
    • M01AE17 dexketoprofen
申请类型
  • TypeLevel1：[not specified]
  • TypeLevel2：[not specified]
  • TypeLevel3：[not specified]
  • TypeLevel4：[not specified]
  • TypeLevel5：[not specified]
附件文件下载
市场状态Positive
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