欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号NL/H/5783/001
药品名称Calcitriol Devatis, 0.25 mcg soft capsules
活性成分
    • calcitriol 0.25 µg
剂型Capsule, soft
上市许可持有人Devatis GmbH Spitalstrasse 22 79539 Loerrach Baden-Wuerttemberg Germany
参考成员国 - 产品名称Netherlands (NL)
Calcitriol Devatis 0,25 microgram, zachte capsules
互认成员国 - 产品名称
    • Germany (DE)
      Calcitriol Devatis 0,25 Mikrogramm Weichkapseln
许可日期2024/05/14
最近更新日期2024/05/14
药物ATC编码
    • A11CC04 calcitriol
申请类型
  • TypeLevel1：Abridged
  • TypeLevel2：Initial Application
  • TypeLevel3：Hybrid application (Art 10.3 Dir 2001/83/EC)
  • TypeLevel4：Chemical Substance
  • TypeLevel5：Prescription Only
附件文件下载
    市场状态Withdrawn（注：已撤市）
    撤市原因：1.The company decided to withdraw the application. At the time of withdrawal, the MS considered that the data provided did not allow to conclude on a positive benefit-risk balance as major objections were raised.
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