欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
SE/H/1114/002
药品名称
Amlodipin Aurobindo
活性成分
Amlodipine besilate 10.0 mg
剂型
Tablet
上市许可持有人
Aurobindo Pharma (Malta) Limited
参考成员国 - 产品名称
Sweden (SE)
互认成员国 - 产品名称
Germany (DE)
Amlodipin Aurobindo 10 mg Tabletten
Italy (IT)
Malta (MT)
Amlodipine Aurobindo 10mg
Netherlands (NL)
许可日期
2011/04/21
最近更新日期
2024/11/19
药物ATC编码
C08CA01 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
PubAR Summary
|
https___www_lakemedelsverket_se_sv_sok_lakemedelsfakta_lakemedel_id_20080930000053
Date of last change:2024/09/06
Final PL
|
SE_H_1114_002_Final PL
Date of last change:2024/09/06
Final SPC
|
SE_H_1114_002_Final SPC
Date of last change:2024/09/06
PubAR
|
SE_H_1114_002_PAR
Date of last change:2024/09/06
Final PL
|
TEST
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase