欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号BE/H/0277/001
药品名称Duogestan 1mg/200mg
活性成分
    • estradiol hemihydrate 1.0 mg
    • progesterone 200.0 mg
剂型capsule soft und tablet
上市许可持有人Besins Healthcare SA Avenue Louise 287 1050 Brussels Belgium
参考成员国 - 产品名称Belgium (BE)
互认成员国 - 产品名称
    • Bulgaria (BG)
      DUOGESTAN 1 mg/ 200 mg
    • Czechia (CZ)
      Duogestan 1mg/200mg
    • Croatia (HR)
      Duogestan 1 mg/200 mg tableta i meka kapsula
    • Estonia (EE)
    • Germany (DE)
      Duogestan 1 mg/200 mg
    • Hungary (HU)
    • Ireland (IE)
    • Lithuania (LT)
      -
    • Latvia (LV)
    • Netherlands (NL)
    • Poland (PL)
      Duogestan
    • Romania (RO)
      Duogestan 1 mg/200 mg
    • Slovenia (SI)
    • Slovakia (SK)
    • United Kingdom (GB)
许可日期2020/12/22
最近更新日期2021/11/15
药物ATC编码
    • G03FA04 progesterone and estrogen
申请类型
  • TypeLevel1:Known Active Substance
  • TypeLevel2:Initial Application
  • TypeLevel3:Bibliographic Art 10 a Dir 2001/83/EC
  • TypeLevel4:Chemical Substance
  • TypeLevel5:Prescription Only
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