欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号SE/H/0836/001
药品名称Lutinus
活性成分
    • Progesterone 100.0 mg
剂型Vaginal tablet
上市许可持有人Ferring Läkemedel AB Sweden
参考成员国 - 产品名称Sweden (SE)
互认成员国 - 产品名称
    • Germany (DE)
      ENDOMETRIN
    • Denmark (DK)
      Lutinus
    • Netherlands (NL)
      Endometrin 100 mg, tabletten voor vaginaal gebruik
    • Iceland (IS)
    • United Kingdom (Northern Ireland) (XI)
    • Ireland (IE)
    • Greece (GR)
    • Norway (NO)
    • Finland (FI)
    • Poland (PL)
    • Hungary (HU)
      LUTINUS 100 mg hüvelytabletta
    • Bulgaria (BG)
      Lutinus
    • Romania (RO)
      LUTINUS 100 mg comprimate vaginale
许可日期2009/11/20
最近更新日期2024/09/11
药物ATC编码
    • G03DA04 progesterone
申请类型
  • TypeLevel1:Known Active Substance
  • TypeLevel2:Initial Application
  • TypeLevel3:Full Dossier Art 8.3(i) 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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