欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
CZ/H/0100/001
药品名称
Lorista 50
活性成分
losartan potassium salt 50.0 mg
剂型
Film-coated tablet
上市许可持有人
KRKA d.d. Šmarješka cesta 6, 8501 Novo mesto Slovenia
参考成员国 - 产品名称
Czechia (CZ)
互认成员国 - 产品名称
Portugal (PT)
Hungary (HU)
Spain (ES)
Norway (NO)
Germany (DE)
Denmark (DK)
Losartankalium "Krka"
Belgium (BE)
United Kingdom (Northern Ireland) (XI)
Austria (AT)
Losartan Krka 50 mg Filmtabletten
France (FR)
Italy (IT)
Sweden (SE)
Latvia (LV)
Bulgaria (BG)
Lorista
Cyprus (CY)
Romania (RO)
Lorista 50 mg comprimate filmate
Iceland (IS)
许可日期
2005/03/02
最近更新日期
2024/07/26
药物ATC编码
C09CA01 losartan
申请类型
TypeLevel1:
Abridged
TypeLevel2:
Initial Application
TypeLevel3:
Generic [Article 10.1.(a)(iii), first paragraph]
TypeLevel4:
Chemical Substance
TypeLevel5:
Prescription Only
附件文件下载
Final PL
|
common_combined_1
Date of last change:2024/09/06
Final Product Information
|
common_combined_clean
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase