欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
SE/H/0406/004
药品名称
Diovan
活性成分
valsartan 160.0 mg
剂型
Film-coated tablet
上市许可持有人
Novartis Sverige AB, Sweden
参考成员国 - 产品名称
Sweden (SE)
互认成员国 - 产品名称
Croatia (HR)
Bulgaria (BG)
Diovan
Cyprus (CY)
Estonia (EE)
France (FR)
Hungary (HU)
Latvia (LV)
Lithuania (LT)
Diovan 160 mg plėvele dengtos tabletės
Malta (MT)
Germany (DE)
Norway (NO)
Netherlands (NL)
Poland (PL)
Diovan
Luxembourg (LU)
Romania (RO)
Diovan 160 mg comprimate filmate
Ireland (IE)
Slovenia (SI)
Austria (AT)
Diovan 160 mg Filmtabletten
Spain (ES)
Portugal (PT)
Italy (IT)
Greece (GR)
Finland (FI)
Belgium (BE)
许可日期
2008/04/05
最近更新日期
2024/02/29
药物ATC编码
C09CA03 valsartan
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 PL
|
SE/H/0406/004_Final PL
Date of last change:2014/01/15
Final SPC
|
SE/H/0406/004_Final SPC
Date of last change:2014/01/15
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase