欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/0701/001
药品名称Yasminelle, filmomhulde tabletten 0,02 mg/3 mg
活性成分
    • Drospirenone 3.0 mg
    • Ethinylestradiol 0.02 mg
剂型Film-coated tablet
上市许可持有人Bayer B.V. Energieweg 1 3641 RT Mijdrecht The Netherlands
参考成员国 - 产品名称Netherlands (NL)
Yasminelle, filmomhulde tabletten 0,02 mg/3 mg
互认成员国 - 产品名称
    • Germany (DE)
    • Belgium (BE)
    • Luxembourg (LU)
    • Ireland (IE)
    • Austria (AT)
      Yasminelle 0,02 mg/3 mg Filmtabletten
    • France (FR)
    • Spain (ES)
    • Portugal (PT)
    • Italy (IT)
    • Greece (GR)
    • Sweden (SE)
    • Norway (NO)
    • Finland (FI)
    • Poland (PL)
      YASMINELLE
    • Latvia (LV)
      Yasminelle 0,02 mg/3 mg apvalkotās tabletes
    • Lithuania (LT)
      Yasminelle 0,02 mg/ 3 mg plėvele dengtos tabletės
    • Estonia (EE)
    • Cyprus (CY)
    • Czechia (CZ)
    • Slovenia (SI)
    • Malta (MT)
许可日期2006/05/02
最近更新日期2025/02/13
药物ATC编码
    • G03AA12 drospirenone and ethinylestradiol
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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