欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
SE/H/2189/001
药品名称
Thiotepa Abcur
活性成分
Thiotepa 15.0 mg
剂型
Powder for concentrate for solution for injection/infusion
上市许可持有人
Abcur AB
参考成员国 - 产品名称
Sweden (SE)
互认成员国 - 产品名称
Norway (NO)
Finland (FI)
Denmark (DK)
Iceland (IS)
许可日期
2023/06/28
最近更新日期
2025/01/31
药物ATC编码
L01AC01 thiotepa
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
附件文件下载
Final PL
|
Final PL
Date of last change:2024/09/06
Final SPC
|
Final SPC
Date of last change:2024/09/06
PubAR
|
https___www_lakemedelsverket_se_sv_sok_lakemedelsfakta_lakemedel_20210831000016_thiotepa_abcur_15_mg_pulver_till_koncentrat_till_infusionsvatska_losning
Date of last change:2024/09/06
PubAR Summary
|
https___www_lakemedelsverket_se_sv_sok_lakemedelsfakta_lakemedel_20210831000016_thiotepa_abcur_15_mg_pulver_till_koncentrat_till_infusionsvatska_losning_2
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase