欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号NL/H/5409/001
药品名称Solifenacin succinate/Tamsulosin hydrochloride Viatris 6 mg/0.4 mg modified-release tablets
活性成分
    • Solifenacin succinate 6.0 mg
    • Tamsulosin hydrochloride 0.4 mg
剂型Modified-release tablet
上市许可持有人Viatris Limited Damastown Industrial Park, Mulhuddart Dublin 15, Co Dublin Ireland
参考成员国 - 产品名称Netherlands (NL)
Solifenacinesuccinaat/Tamsulosinehydrochloride Viatris 6 mg/0,4 mg, tabletten met gereguleerde afgifte
互认成员国 - 产品名称
    • Belgium (BE)
    • Luxembourg (LU)
    • Spain (ES)
    • Portugal (PT)
    • Italy (IT)
    • Czechia (CZ)
      Solifenacin/Tamsulosin Synthon
许可日期2023/04/26
最近更新日期2025/02/11
药物ATC编码
    • G04CA53 tamsulosin and solifenacin
申请类型
  • TypeLevel1：Abridged
  • TypeLevel2：Initial Application
  • TypeLevel3：Generic Art 10.1 and 10.2 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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