欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
DK/H/1517/002
药品名称
Valsartan Teva
活性成分
valsartan 80.0 mg
剂型
Film-coated tablet
上市许可持有人
Teva B.V. Swensweg 5 2031 GA Haarlem The Netherlands
参考成员国 - 产品名称
Denmark (DK)
互认成员国 - 产品名称
Netherlands (NL)
Ireland (IE)
France (FR)
Spain (ES)
Portugal (PT)
Poland (PL)
Bespres
Hungary (HU)
VALSARTAN-TEVA 80 mg filmtabletta
许可日期
2009/06/30
最近更新日期
2024/02/01
药物ATC编码
C09CA03 valsartan
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
PAR
|
parmod5_dk1517valsartanteva_pdf
Date of last change:2022/06/02
Final PL
|
common_pl_clean
Date of last change:2022/06/02
Final SPC
|
common_spc_clean
Date of last change:2022/06/02
Final Labelling
|
1.3.1 combined labelling-40mg-eu clean
Date of last change:2018/02/08
Final Labelling
|
1.3.1 combined labelling-80mg-eu clean
Date of last change:2018/02/08
Final Labelling
|
1.3.1 combined labelling-160mg-eu clean
Date of last change:2018/02/08
Final Labelling
|
1.3.1 combined labelling-320mg-eu clean
Date of last change:2018/02/08
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase