欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
IT/H/0965/002
药品名称
Telmisartan Sandoz 40 mg
活性成分
Telmisartan 20.0 mg
剂型
Tablet
上市许可持有人
Sandoz B.V. Veluwezoom 22 1327 AH Almere
参考成员国 - 产品名称
Italy (IT)
互认成员国 - 产品名称
Netherlands (NL)
Telmisartan Sandoz 40 mg, tabletten
许可日期
2011/03/11
最近更新日期
2024/11/27
药物ATC编码
C09CA07 telmisartan
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 Product Information
|
common_outer _ 1_193 _ NLH1821 _ RVG105913_4_5
Date of last change:2024/09/06
Final Labelling
|
common_outer telmisartan sadoz 1821
Date of last change:2024/09/06
Final Product Information
|
common_pl _ NLH1821 _ RVG105913_4_5
Date of last change:2024/09/06
Final PL
|
common_pl 1821
Date of last change:2024/09/06
Final Labelling
|
common_pl telmisartan sandoz 1821
Date of last change:2024/09/06
Final Product Information
|
common_spc
Date of last change:2024/09/06
Final Labelling
|
common_spc telmisartan sandoz 1821
Date of last change:2024/09/06
Final SPC
|
common_spc_2
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase