欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
NL/H/5091/001
药品名称
Exemestan Sandoz
活性成分
Exemestane 25.0 mg
剂型
Film-coated tablet
上市许可持有人
Sandoz B.V. Hospitaaldreef 29 1315 RC Almere Nederland
参考成员国 - 产品名称
Netherlands (NL)
互认成员国 - 产品名称
Germany (DE)
France (FR)
Italy (IT)
Sweden (SE)
Norway (NO)
Belgium (BE)
Spain (ES)
许可日期
2010/04/22
最近更新日期
2025/02/07
药物ATC编码
L02BG06 exemestane
申请类型
TypeLevel1:
[not specified]
TypeLevel2:
[not specified]
TypeLevel3:
[not specified]
TypeLevel4:
[not specified]
TypeLevel5:
[not specified]
附件文件下载
Final Labelling
|
1_3_1 spc_label_pl _ common_outer _ 5_236 _ Clean
Date of last change:2024/09/06
Final PL
|
1_3_1 spc_label_pl _ common_pl _ 10_781 _ Clean
Date of last change:2024/09/06
Final SPC
|
1_3_1 spc_label_pl _ common_spc _ 10_224 _ Clean
Date of last change:2024/09/06
PubAR
|
parmod5_dk1732exemestansandoz_pdf
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase