欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号FI/H/0910/001
药品名称Emtricitabine/Tenofovir disoproxil Sandoz
活性成分
    • Emtricitabine 200.0 mg
    • Tenofovir 245.0 mg
剂型Film-coated tablet
上市许可持有人Sandoz A/S Edvard Thomsens Vej 14 2300 Copenhagen S Denmark
参考成员国 - 产品名称Finland (FI)
互认成员国 - 产品名称
    • Denmark (DK)
    • Netherlands (NL)
    • Iceland (IS)
      Emtricitabine/Tenofovir disoproxil Sandoz 200 mg/245 mg filmuhúðuð tafla
    • United Kingdom (Northern Ireland) (XI)
    • Austria (AT)
      Emtricitabin/Tenofovir Sandoz 200 mg/245 mg - Filmtabletten
    • France (FR)
    • Italy (IT)
    • Sweden (SE)
    • Norway (NO)
    • Lithuania (LT)
      Emtricitabine / Tenofovir disoproxil Sandoz 200 mg / 245 mg plėvele dengtos tabletės
    • Estonia (EE)
      EMTRICITABINE/TENOFOVIR DISOPROXIL SANDOZ
    • Hungary (HU)
    • Romania (RO)
许可日期2017/03/16
最近更新日期2025/02/03
药物ATC编码
    • J05AR03 tenofovir disoproxil and emtricitabine
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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