欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
SE/H/2143/002
药品名称
Amlodipin/Valsartan Teva
活性成分
amlodipine besilate 5.0 mg
valsartan 160.0 mg
剂型
Film-coated tablet
上市许可持有人
Teva B.V. Netherlands
参考成员国 - 产品名称
Sweden (SE)
互认成员国 - 产品名称
Netherlands (NL)
Amlodipine/Valsartan Teva 5 mg/160 mg, filmomhulde tabletten
France (FR)
Portugal (PT)
Lithuania (LT)
-
许可日期
2022/04/19
最近更新日期
2022/08/12
药物ATC编码
C09DB01 valsartan and amlodipine
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 Summary
|
https___www_lakemedelsverket_se_sv_sok_lakemedelsfakta_lakemedel_id_20210331000240_2
Date of last change:2022/09/27
PAR
|
https___www_lakemedelsverket_se_sv_sok_lakemedelsfakta_lakemedel_id_20210331000240
Date of last change:2022/09/27
Final PL
|
Final SPC
|
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase