欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号
IT/H/0965/003
药品名称
Telmisartan Sandoz 80 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 80 mg, tabletten
许可日期
2011/03/11
最近更新日期
2025/02/04
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 SPC
|
1_3_1 spc_label_pl _ common_spc _ 6_137 clean
Date of last change:2024/09/06
Final Labelling
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common_outer telmisartan sadoz 1821
Date of last change:2024/09/06
Final PL
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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 Labelling
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common_spc telmisartan sandoz 1821
Date of last change:2024/09/06
Final Product Information
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nlh1801_4_15_ 21_common_PI
Date of last change:2024/09/06
Final Product Information
|
nlh1801_4_15_ 21_common_PI _ clean version
Date of last change:2024/09/06
Final Product Information
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nlh1801_4_15_ 21_common_SPC
Date of last change:2024/09/06
Final Product Information
|
nlh1801_4_15_ 21_common_SPC _ clean version
Date of last change:2024/09/06
Final Product Information
|
nlh2603_4_2705_common_Pl
Date of last change:2024/09/06
Final Product Information
|
nlh2603_4_2705_common_Pl _ clean version
Date of last change:2024/09/06
Final Product Information
|
nlh2603_4_2705_common_SPC
Date of last change:2024/09/06
Final Product Information
|
nlh2603_4_2705_common_SPC _ clean version
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase