欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号SE/H/0150/001
药品名称Activelle
活性成分
    • estradiol hemihydrate 1.0 mg
    • norethisterone acetate 0.5 mg
剂型Film-coated tablet
上市许可持有人Novo Nordisk A/S Denmark
参考成员国 - 产品名称Sweden (SE)
互认成员国 - 产品名称
    • Germany (DE)
    • Denmark (DK)
    • Belgium (BE)
    • Luxembourg (LU)
    • Iceland (IS)
    • United Kingdom (Northern Ireland) (XI)
    • Ireland (IE)
    • Austria (AT)
      Activelle 1 mg/0,5 mg Filmtabletten
    • France (FR)
    • Spain (ES)
    • Portugal (PT)
    • Italy (IT)
    • Norway (NO)
    • Finland (FI)
    • Latvia (LV)
    • Lithuania (LT)
      Activelle 1mg/0,5mg plėvele dengtos tabletės
    • Estonia (EE)
    • Hungary (HU)
      ACTIVELLE filmtabletta
    • Bulgaria (BG)
      Activelle
    • Czechia (CZ)
    • Slovakia (SK)
    • Netherlands (NL)
    • Croatia (HR)
      Activelle 1 mg/0,5 mg filmom obložene tablete
    • Slovenia (SI)
许可日期1998/07/06
最近更新日期2024/04/23
药物ATC编码
    • G03FA01 norethisterone and estrogen
申请类型
  • TypeLevel1:Known Active Substance
  • TypeLevel2:Initial Application
  • TypeLevel3:Full Dossier Article 4.8 Di 65/65
  • TypeLevel4:Chemical Substance
  • TypeLevel5:Prescription Only
附件文件下载
市场状态Positive
©2006-2024 Drugfuture->European Union HMA Authorisation of Medicines DataBase