欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号
DE/H/6047/002
药品名称
Telmisartan-ratiopharm 40 mg Tabletten
活性成分
Telmisartan 20.0 mg
剂型
Tablet
上市许可持有人
ratiopharm GmbH Graf-Arco-Strasse 3 89079 Ulm Germany
参考成员国 - 产品名称
Germany (DE)
互认成员国 - 产品名称
Portugal (PT)
Belgium (BE)
Luxembourg (LU)
United Kingdom (Northern Ireland) (XI)
Austria (AT)
Telmisartan ratiopharm 40 mg Tabletten
Spain (ES)
Italy (IT)
Finland (FI)
Latvia (LV)
Lithuania (LT)
Telmisartan-ratiopharm 40mg tabletės
Estonia (EE)
TELMISARTAN-RATIOPHARM 40MG
Hungary (HU)
TELMISARTAN-RATIOPHARM 40 mg tabletta
许可日期
2010/06/19
最近更新日期
2024/11/14
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
|
m1_3_1_spc_telmisartan20mg_pl15773_0821_clean
Date of last change:2024/09/06
Final SPC
|
m1_3_1_spc_telmisartan20mg_pl15773_0821_tracked
Date of last change:2024/09/06
Final SPC
|
m1_3_1_spc_telmisartan40mg_pl15773_0822_clean
Date of last change:2024/09/06
Final SPC
|
m1_3_1_spc_telmisartan40mg_pl15773_0822_tracked
Date of last change:2024/09/06
Final SPC
|
m1_3_1_spc_telmisartan80mg_pl15773_0823_clean
Date of last change:2024/09/06
Final SPC
|
m1_3_1_spc_telmisartan80mg_pl15773_0823_tracked
Date of last change:2024/09/06
Final PL
|
FINAL PI DE_6047_001_003_P_002
Date of last change:2024/09/06
Final Product Information
|
final_common_comb Lab_6047_035
Date of last change:2024/09/06
Final Product Information
|
final_common_PL_6047_035
Date of last change:2024/09/06
Final Product Information
|
final_common_SPC_6047_035
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase