欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号SE/H/0481/003
药品名称Fosrenol
活性成分
    • lanthanum(III)carbonate 750.0 mg
剂型Chewable tablet
上市许可持有人Takeda Pharmaceuticals International AG Ireland Branch
参考成员国 - 产品名称Sweden (SE)
互认成员国 - 产品名称
    • Italy (IT)
    • Greece (GR)
    • Norway (NO)
    • Finland (FI)
    • Latvia (LV)
    • Estonia (EE)
      FOSRENOL
    • Hungary (HU)
      FOSRENOL 750 mg rágótabletta
    • Bulgaria (BG)
      Fosrenol
    • Cyprus (CY)
    • Slovakia (SK)
      Fosrenol 750 mg žuvacie tablety
    • Slovenia (SI)
    • Malta (MT)
    • Lithuania (LT)
      FOSRENOL 750 mg kramtomosios tabletės
    • Germany (DE)
    • Denmark (DK)
    • Belgium (BE)
    • Netherlands (NL)
    • Luxembourg (LU)
    • Iceland (IS)
    • Ireland (IE)
    • Austria (AT)
      Fosrenol 750 mg Kautabletten
    • France (FR)
    • Spain (ES)
许可日期2005/03/01
最近更新日期2024/07/18
药物ATC编码
    • V03AE03 lanthanum carbonate
申请类型
  • TypeLevel1：New Active Substance
  • TypeLevel2：Additional Strength/Form
  • TypeLevel3：Full Dossier [Article 8.3(i)]
  • TypeLevel4：Chemical Substance
  • TypeLevel5：Prescription Only
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市场状态Positive
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