欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/3168/001
药品名称Cortiment 9 mg, prologed release tablets
活性成分
    • budesonide 9.0 mg
剂型Prolonged-release tablet
上市许可持有人Ferring B.V. Polarisavenue 130 2132 JX HOOFDDORP
参考成员国 - 产品名称Netherlands (NL)
Cortiment 9 mg, prolonged releales tablets
互认成员国 - 产品名称
    • Denmark (DK)
    • France (FR)
    • Germany (DE)
      CORTIMENT MMX 9 mg Retardtabletten
    • Iceland (IS)
      Cortiment 9 mg Forðatafla
    • United Kingdom (Northern Ireland) (XI)
    • Ireland (IE)
    • Austria (AT)
      CortimentMMX 9 mg - Retardtabletten
    • Portugal (PT)
    • Italy (IT)
    • Greece (GR)
      CORTIMENT
    • Sweden (SE)
    • Norway (NO)
      Cortiment
    • Finland (FI)
    • Poland (PL)
      Cortiment MMX
    • Latvia (LV)
    • Lithuania (LT)
      Budesonide Ferring 9 mg pailginto atpalaidavimo tabetės
    • Estonia (EE)
      CORTIMENT
    • Hungary (HU)
      CORTIMENT 9 mg retard tabletta
    • Bulgaria (BG)
      Cortiment
    • Cyprus (CY)
      CORTIMENT PR TABS
    • Czechia (CZ)
      Cortiment 9 MG
    • Romania (RO)
      CORTIMENT 9 mg comprimate cu eliberare prelungita
    • Slovakia (SK)
      CortimentMMX
    • Slovenia (SI)
    • Malta (MT)
      CortimentMMX 9mg Prolonged release tablet
    • Croatia (HR)
      Cortiment MMX 9 mg tablete s produljenim oslobađanjem
许可日期2014/10/17
最近更新日期2024/01/25
药物ATC编码
    • A07EA06 budesonide
申请类型
  • TypeLevel1:Known Active Substance
  • TypeLevel2:Initial Application
  • TypeLevel3:Other Generic application Art 10.3 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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