欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号HU/H/0169/002
药品名称Tolterodin-Teva
活性成分
    • tolterodine tartrate 2.0 mg
剂型Film-coated tablet
上市许可持有人Biogal-Teva Pharma Zrt. Rákóczi út 70-72. Budapest H-1074
参考成员国 - 产品名称Hungary (HU)
Tolterodin-TEVA 2 mg filmtabletta
互认成员国 - 产品名称
    • Germany (DE)
    • Netherlands (NL)
    • Luxembourg (LU)
    • United Kingdom (Northern Ireland) (XI)
    • Austria (AT)
      Tolterodin ratiopharm 2 mg Filmtabletten
    • France (FR)
    • Greece (GR)
    • Sweden (SE)
      Tolterodine Teva
    • Poland (PL)
      Defur
    • Lithuania (LT)
      Tolterodine Teva 2 mg plėvele dengtos tabletės
许可日期2008/10/02
最近更新日期2012/08/09
药物ATC编码
    • G04BD07 tolterodine
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
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    市场状态Positive
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