欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号DK/H/1729/001
药品名称Exemestan Accord
活性成分
    • exemestane 25.0 mg
剂型Film-coated tablet
上市许可持有人Accord Healthcare B.V. Winthontlaan 200 Utrecht 3526 KV Netherlands
参考成员国 - 产品名称Denmark (DK)
Exemestan "Accord"
互认成员国 - 产品名称
    • Germany (DE)
      Exemestane Accord 25mg Filmtabletten
    • Netherlands (NL)
    • Ireland (IE)
    • France (FR)
    • Spain (ES)
    • Italy (IT)
    • Greece (GR)
    • Latvia (LV)
      Exemestane Accord 25 mg apvalkotās tabletes
    • Lithuania (LT)
      Exemestane Accord 25 mg plėvele dengtos tabletės
    • Estonia (EE)
      EXEMESTANE ACCORD
    • Bulgaria (BG)
      Exemestane Accord
    • Czechia (CZ)
      Exemestane Accord 25 mg Potahované tablety
    • Romania (RO)
      Exemestan Accord 25 mg comprimate filmate
    • United Kingdom (Northern Ireland) (XI)
许可日期2010/04/22
最近更新日期2024/04/24
药物ATC编码
    • L02BG06 exemestane
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
附件文件下载
市场状态Positive
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