欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
AT/H/0958/002
药品名称
CandAm16 mg/5 mg Hartkapseln
活性成分
Amlodipine besilate 6.94 mg
candesartancilexetil 16.0 mg
剂型
Capsule, hard
上市许可持有人
Genericon Pharma GmbH
参考成员国 - 产品名称
Austria (AT)
CandAm
互认成员国 - 产品名称
许可日期
2019/02/19
最近更新日期
2024/11/22
药物ATC编码
C09DB07 candesartan and amlodipine
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 SPC
|
FI_20_03_06_CandAm_tr
Date of last change:2024/09/06
Final SPC
|
FI_21_11_22_CandAm_cl
Date of last change:2024/09/06
Final PL
|
GI_20_03_06_CandAm_UA_tr
Date of last change:2024/09/06
Final PL
|
GI_21_11_22_CandAm_UA_cl
Date of last change:2024/09/06
Final Labelling
|
KE_18_07_26_CandAm_16_10
Date of last change:2024/09/06
Final Labelling
|
KE_18_07_26_CandAm_16_5
Date of last change:2024/09/06
Final Labelling
|
KE_18_07_26_CandAm_8_10
Date of last change:2024/09/06
Final Labelling
|
KE_18_07_26_CandAm_8_5
Date of last change:2024/09/06
PubAR
|
updated PAR_AT_H_0958_001_004
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase