欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号SE/H/2023/001
药品名称Utrogestan
活性成分
    • progesterone 200.0 mg
剂型Vaginal capsule, soft
上市许可持有人Besins Healthcare Ireland Limited Ireland
参考成员国 - 产品名称Sweden (SE)
互认成员国 - 产品名称
    • Portugal (PT)
    • Italy (IT)
    • Malta (MT)
      Utrogestan Vaginal 200 mg Capsules, soft
    • Denmark (DK)
    • Iceland (IS)
    • United Kingdom (Northern Ireland) (XI)
    • Netherlands (NL)
      Utrogestan 200 mg, zachte capsules voor vaginaal gebruik
    • Ireland (IE)
    • Norway (NO)
    • Poland (PL)
      Utrogestan
    • Latvia (LV)
      Progesterone Besins 200 mg mīkstās vaginālās kapsulas
    • Lithuania (LT)
      -
    • Estonia (EE)
    • Hungary (HU)
      UTROGESTAN 200 mg lágy hüvelykapszula
    • Bulgaria (BG)
    • Czechia (CZ)
      Uterogestan
    • Slovakia (SK)
    • Slovenia (SI)
    • Croatia (HR)
    • Spain (ES)
许可日期2019/03/05
最近更新日期2024/03/18
药物ATC编码
    • G03DA04 progesterone
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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