欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
SE/H/0568/001
药品名称
Matrifen
活性成分
Fentanyl 25.0 µg
剂型
Transdermal patch
上市许可持有人
Takeda Pharma AB Sweden
参考成员国 - 产品名称
Sweden (SE)
Matrifen
互认成员国 - 产品名称
Denmark (DK)
Belgium (BE)
Luxembourg (LU)
United Kingdom (Northern Ireland) (XI)
Ireland (IE)
Spain (ES)
Italy (IT)
Greece (GR)
Finland (FI)
Poland (PL)
Matrifen
Latvia (LV)
Lithuania (LT)
matrifen 12 mikrogramų/val. transderminiai pleistrai
Estonia (EE)
MATRIFEN
Hungary (HU)
Matrifen 12 mikrogramm/h transzdermális tapasz
Czechia (CZ)
Matrifen 12 mcg/h
许可日期
2006/08/04
最近更新日期
2024/10/02
药物ATC编码
N02AB03 fentanyl
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
|
SE_H_0568_001_Final PL
Date of last change:2024/09/06
Final SPC
|
SE_H_0568_001_Final SPC
Date of last change:2024/09/06
PubAR
|
SE_H_0568_001_PAR
Date of last change:2024/09/06
市场状态
Positive
©2006-2024
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European Union HMA Authorisation of Medicines DataBase