欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
PT/H/0964/003
药品名称
Telmisartan Pentafarma
活性成分
telmisartan 80.0 mg
剂型
Tablet
上市许可持有人
Pentafarma - Sociedade Técnico-Medicinal, S.A. PT
参考成员国 - 产品名称
Portugal (PT)
互认成员国 - 产品名称
Italy (IT)
许可日期
2013/08/22
最近更新日期
2024/08/18
药物ATC编码
C09CA07 telmisartan
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
PubAR
|
0964_Telmisartan_Pentafarma__PAR_genericos_Final_04JUL2018
Date of last change:2024/09/06
Final PL
|
leaflet_20mg_proposed_RAS_RSI_clean
Date of last change:2024/09/06
Final PL
|
leaflet_40mg_proposed_RAS_RSI_clean
Date of last change:2024/09/06
Final PL
|
leaflet_80mg_proposed_RAS_RSI_clean
Date of last change:2024/09/06
Final SPC
|
smpc_20mg_proposed_RAS_RSI_clean_03mar15
Date of last change:2024/09/06
Final SPC
|
smpc_40mg_proposed_RAS_RSI_clean_03mar15
Date of last change:2024/09/06
Final SPC
|
smpc_80mg_proposed_RAS_RSI_clean_03mar15
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase