欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
NL/H/2431/002
药品名称
Blastomat 20mg Capsules, harde
活性成分
temozolomide 20.0 mg
剂型
Capsule, hard
上市许可持有人
Alvogen IPCo S.a.r.l
参考成员国 - 产品名称
Netherlands (NL)
Blastomat 20 mg capsules, harde
互认成员国 - 产品名称
Estonia (EE)
Lithuania (LT)
Blastomat 20 mg kietosios kapsulės
Latvia (LV)
许可日期
2012/09/26
最近更新日期
2024/05/14
药物ATC编码
L01AX03 temozolomide
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 Product Information
|
common combined_common_combined
Date of last change:2024/09/06
Final Labelling
|
common_temozolomide_5mg20mg100mg140mg180mg250mg_hcaps_eirgen_lab_v_07_clean
Date of last change:2024/09/06
Final PL
|
common_temozolomide_5mg20mg100mg140mg180mg250mg_hcaps_eirgen_pl_v_07_clean
Date of last change:2024/09/06
Final SPC
|
common_temozolomide_5mg20mg100mg140mg180mg250mg_hcaps_eirgen_spc_v_011_clean
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase