欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
DK/H/3422/002
药品名称
Cabozantinib Teva
活性成分
cabozantinib L-malate 40.0 mg
剂型
Film-coated tablet
上市许可持有人
Teva B.V. Swensweg 5 2031GA Haarlem Netherlands
参考成员国 - 产品名称
Denmark (DK)
Cabozantinib Teva
互认成员国 - 产品名称
France (FR)
Italy (IT)
Finland (FI)
Czechia (CZ)
Cabozantinib Teva
Croatia (HR)
许可日期
2025/05/28
最近更新日期
2025/05/28
药物ATC编码
L01EX07 cabozantinib
申请类型
TypeLevel1:
Abridged
TypeLevel2:
Additional Strength/Form
TypeLevel3:
Generic Art 10.1 and 10.2 Dir 2001/83/EC
TypeLevel4:
Chemical Substance
TypeLevel5:
Prescription Only
附件文件下载
PubAR Summary
|
PAR_Summary_Cabozantinib Teva_DK_H_3422_001_003_DC
Date of last change:2025/09/08
PubAR
|
PAR_Scientific discussion_Cabozantinib Teva_DK_H_3422_001_003_DC
Date of last change:2025/09/08
Final Labelling
|
Module 1_3_1 label
Date of last change:2025/05/28
Final PL
|
cabozantinib_pil_responses_to_day_180_195_clean
Date of last change:2025/05/28
Final SPC
|
cabozantinib_smpc_responses_to_day_180_195_clean
Date of last change:2025/05/28
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase