欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/4119/001
药品名称Tenofovir disoproxil AHCL 245 mg film-coated tablets
活性成分
    • Tenofovir disoproxil fumarate 300.0 mg
剂型Film-coated tablet
上市许可持有人Accord Healthcare B.V. Winthontlaan 200 3508 AD Utrecht The Netherlands
参考成员国 - 产品名称Netherlands (NL)
Tenofovir disoproxil Accordpharma 245 mg filmomhulde tabletten
互认成员国 - 产品名称
    • Denmark (DK)
    • United Kingdom (Northern Ireland) (XI)
    • Austria (AT)
      Tenofovir disoproxil Accordpharma 245 mg Filmtabletten
    • Spain (ES)
    • Greece (GR)
    • Sweden (SE)
    • Norway (NO)
    • Finland (FI)
    • Poland (PL)
      Tenofovir disoproxil Accordpharma
    • Hungary (HU)
      TENOFOVIR DISOPROXIL ACCORDPHARMA 245 mg filmtabletta
    • Bulgaria (BG)
      Tenofovir Disoproxil AHCL
    • Czechia (CZ)
      Tenofovir disoproxil AHCL 245 mg potahované tablety
    • Romania (RO)
      Tenofovir Disoproxil Accordpharma 245 mg comprimate filmate
许可日期2018/10/01
最近更新日期2024/10/22
药物ATC编码
    • J05AF07 tenofovir disoproxil
申请类型
  • TypeLevel1:Known Active Substance
  • 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
©2006-2024 Drugfuture->European Union HMA Authorisation of Medicines DataBase