欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号CZ/H/0195/001
药品名称Bicalutamidum Genthon 50 mg, film-coated tablets
活性成分
    • bicalutamide 50.0 mg
剂型Film-coated tablet
上市许可持有人Genthon BV P.O. Box 7071 6503 GN Nijmegen, The Netherlands change RMS NL/H/2299
参考成员国 - 产品名称Czechia (CZ)
互认成员国 - 产品名称
    • Germany (DE)
    • Netherlands (NL)
    • United Kingdom (Northern Ireland) (XI)
    • Austria (AT)
    • Spain (ES)
    • Portugal (PT)
    • Italy (IT)
    • Greece (GR)
    • Norway (NO)
    • Finland (FI)
    • Lithuania (LT)
    • Hungary (HU)
    • Romania (RO)
许可日期2008/06/30
最近更新日期2019/03/11
药物ATC编码
    • L02BB03 bicalutamide
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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