欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号SE/H/2242/001
药品名称Utrogestan
活性成分
    • progesterone 300.0 mg
剂型Vaginal capsule, soft
上市许可持有人Besins Healthcare Ireland Ltd. 16 Pembroke Street Upper DUBLIN 2, D02 HE63 IRELAND
参考成员国 - 产品名称Sweden (SE)
互认成员国 - 产品名称
    • Malta (MT)
    • Luxembourg (LU)
    • Iceland (IS)
    • Ireland (IE)
    • France (FR)
    • Spain (ES)
    • Norway (NO)
      Utrogestan
    • Portugal (PT)
    • Latvia (LV)
      Progesterone Besins 300 mg mīkstās vaginālās kapsulas
    • Italy (IT)
    • Estonia (EE)
      UTROGESTAN
    • Poland (PL)
      Utrogestan
    • Hungary (HU)
    • Lithuania (LT)
      Progesterone Besins 300 mg makšties minkštosios kapsulės
    • Bulgaria (BG)
      Utrogestan
    • Cyprus (CY)
      Utrogestan Κολπικό 300 mg καψάκιο, μαλακό
    • Slovakia (SK)
    • Czechia (CZ)
      Utrogestan
    • Finland (FI)
      Lugesteron
    • Belgium (BE)
      Utrogestan Vaginal 300 mg capsules molles
    • Slovenia (SI)
    • Netherlands (NL)
    • Croatia (HR)
      Utrogestan 300 mg meke kapsule za rodnicu
    • Denmark (DK)
      Progestan
许可日期2021/04/07
最近更新日期2023/12/07
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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