欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
PT/H/2610/004
药品名称
Sunitinib Bluepharma
活性成分
SUNITINIB 50.0 mg
剂型
Capsule, hard
上市许可持有人
Bluepharma Genéricos - Comercio de Medicamentos, S.A
参考成员国 - 产品名称
Portugal (PT)
互认成员国 - 产品名称
Cyprus (CY)
Sunitinib Pharmascience 50mg hard capsules
Slovenia (SI)
Croatia (HR)
Sunitinib Pharmascience 50 mg tvrde kapsule
Poland (PL)
Sunitinib Pharmascience
Hungary (HU)
Sunitinib Pharmascience 50 mg kemény kapszula
Bulgaria (BG)
Sunitinib Pharmascience
许可日期
2021/08/10
最近更新日期
2024/06/28
药物ATC编码
L01XE04 sunitinib
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
|
common_pl_proposed_clean
Date of last change:2024/09/06
Final SPC
|
pt_spc_proposed_clean
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase