欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
SE/H/0406/005
药品名称
Diovan
活性成分
valsartan 40.0 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
Latvia (LV)
Austria (AT)
Bulgaria (BG)
Cyprus (CY)
Estonia (EE)
France (FR)
Malta (MT)
Norway (NO)
Slovenia (SI)
Romania (RO)
Poland (PL)
Germany (DE)
Ireland (IE)
Spain (ES)
Portugal (PT)
Italy (IT)
Greece (GR)
Finland (FI)
Croatia (HR)
Diovan 40 mg filmom obložene tablete
Lithuania (LT)
许可日期
2005/05/04
最近更新日期
2024/02/29
药物ATC编码
C09CA03 valsartan
申请类型
TypeLevel1:
Line Extension
TypeLevel2:
Additional Strength/Form
TypeLevel3:
Full Dossier [Article 8.3(i)]
TypeLevel4:
Chemical Substance
TypeLevel5:
Prescription Only
附件文件下载
Final PL
|
SE/H/0406/005_Final PL
Date of last change:2014/01/15
Final SPC
|
SE/H/0406/005_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