欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
PT/H/2497/001
药品名称
Desloratadin Mylan
活性成分
desloratadine 0.5 mg/ml
剂型
Oral solution
上市许可持有人
Mylan AB P.O. Box 23033 S-10435 Stockholm Sweden
参考成员国 - 产品名称
Portugal (PT)
互认成员国 - 产品名称
Denmark (DK)
Desloratadin Mylan
许可日期
2011/12/22
最近更新日期
2023/03/13
药物ATC编码
R06AX27 desloratadine
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 Product Information
|
common_impack_dk2066_clean_v008
Date of last change:2024/09/06
Final Product Information
|
common_outer_dk2066_clean_v008
Date of last change:2024/09/06
Final Product Information
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common_pl_dk2066_clean_v008rtq
Date of last change:2024/09/06
Final Product Information
|
common_spc_dk2066_clean_v008rtq
Date of last change:2024/09/06
Final Labelling
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Final _ common_outer_dk2066_CLEAN_v020
Date of last change:2024/09/06
Final Labelling
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Final common_impack_dk2066_CLEAN_v020
Date of last change:2024/09/06
Final SPC
|
Final common_spc_dk2066_CLEAN_v020
Date of last change:2024/09/06
Final PL
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Final PL_clean DK_H_2066_IB_021_G Desloratadin Mylan
Date of last change:2024/09/06
PubAR
|
PAR2066_1
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase