欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
NL/H/1940/001
药品名称
Nateran 25 mg
活性成分
exemestane 25.0 mg
剂型
Film-coated tablet
上市许可持有人
Synthon B.V.
参考成员国 - 产品名称
Netherlands (NL)
Nateran 25 mg, filmomhulde tabletten
互认成员国 - 产品名称
Germany (DE)
Nateran 25 mg Filmtabletten
United Kingdom (Northern Ireland) (XI)
Spain (ES)
Italy (IT)
Finland (FI)
Latvia (LV)
Lithuania (LT)
Exemestane SanoSwiss 25 mg plėvele dengtos tabletės
Estonia (EE)
EXEMESTANE SANOSWISS
Hungary (HU)
TEARAN 25 mg filmtabletta
许可日期
2010/12/15
最近更新日期
2024/07/15
药物ATC编码
L02BG06 exemestane
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 Labelling
|
common_combined_ spc
Date of last change:2024/09/06
Final Labelling
|
common_combined_label
Date of last change:2024/09/06
Final Labelling
|
common_combined_pil
Date of last change:2024/09/06
Final Labelling
|
H_Bericht IB variatie MRP_nieuwe richtlijn_
Date of last change:2024/09/06
Final SPC
|
M1_3_1_01_EMT_tab25_001_08_core
Date of last change:2024/09/06
Final PL
|
M1_3_1_03_EMT_tab25_001_09_core
Date of last change:2024/09/06
PubAR
|
PAR_1940_DC_exemestaan_7 feb 2011
Date of last change:2024/09/06
市场状态
Positive
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