欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/0487/003
药品名称Vesicare 1 mg/ml oral suspension
活性成分
    • Solifenacin succinate 1.0 mg/ml
剂型Oral suspension
上市许可持有人Astellas Pharma Europe BV Sylviusweg 62 2333 BE Leiden The Netherlands
参考成员国 - 产品名称Netherlands (NL)
Vesicare 1 mg/ml, suspensie voor oraal gebruik
互认成员国 - 产品名称
    • Germany (DE)
      Vesikur 1 mg/ml Suspension zum Einnehmen
    • Denmark (DK)
      Vesicare
    • Belgium (BE)
      Vesicare 1mg/ml suspensie voor oraal gebruik/ suspension buvable /Suspension zum Einnehmen
    • Luxembourg (LU)
    • Iceland (IS)
      Vesicare 1 mg/ml Mixtúra, dreifa
    • United Kingdom (Northern Ireland) (XI)
    • Ireland (IE)
    • Liechtenstein (LI)
    • Austria (AT)
      Vesicare 1 mg/ml Suspension zum Einnehmen
    • France (FR)
    • Spain (ES)
    • Portugal (PT)
    • Italy (IT)
    • Greece (GR)
      VESICARE
    • Sweden (SE)
    • Norway (NO)
      Vesicare
    • Finland (FI)
    • Poland (PL)
      Vesicare
    • Latvia (LV)
      Vesicare 1 mg/ml suspensija iekšķīgai lietošanai
    • Lithuania (LT)
      Vesicare 1 mg/ml geriamoji suspensija
    • Estonia (EE)
      VESICARE
    • Hungary (HU)
      VESICARE 1 mg/ml belsőleges szuszpenzió
    • Bulgaria (BG)
      Vesicare
    • Cyprus (CY)
      VESICARE ORAL SUSPENSION 1MG/ML
    • Czechia (CZ)
      VESICARE 1 MG/ML PERORÁLNÍ SUSPENZE
    • Romania (RO)
      Vesicare 1 mg/ml suspensie orală
    • Slovakia (SK)
      Vesicare 1 mg/ml perorálna suspenzia
    • Slovenia (SI)
      Vesicare 1mg/ml peroralna suspenzija
    • Malta (MT)
      Vesicare 1 mg/ml oral suspension
    • Croatia (HR)
      Vesicare 1 mg/ml oralna suspenzija
许可日期2015/08/10
最近更新日期2024/09/30
药物ATC编码
    • G04BD08 solifenacin
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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