欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
DE/H/0848/003
药品名称
Losar Teva 50mg Filmtabletten
活性成分
Losartan potassium salt 50.0 mg
剂型
Film-coated tablet
上市许可持有人
TEVA GmbH Graf-Arco-Str. 3 89079 Ulm Germany
参考成员国 - 产品名称
Germany (DE)
互认成员国 - 产品名称
Belgium (BE)
Ireland (IE)
许可日期
2007/10/05
最近更新日期
2024/10/15
药物ATC编码
C09CA01 losartan
申请类型
TypeLevel1:
Abridged
TypeLevel2:
Additional Strength/Form
TypeLevel3:
Generic Art 10.1 and 10.2 Dir 2001/83/EC
TypeLevel4:
Chemical Substance
TypeLevel5:
Prescription Only
附件文件下载
Final PL
|
losartan_de_h_0848_002_004_pil_02_01_24
Date of last change:2024/10/15
Final SPC
|
losartan_de_h_0848_002_004_smpc_02_01_24
Date of last change:2024/10/15
PubAR
|
04_DE_848_1_4_DC_Losartan_Wyvern_final PAR
Date of last change:2024/09/06
Final Product Information
|
Final_common_Package Leaflet
Date of last change:2024/09/06
Final Product Information
|
Final_Common_Summary of Product Characteristi
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase