欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
PT/H/2064/001
药品名称
Parecoxib
活性成分
parecoxib 40.0 mg
剂型
Powder for solution for injection
上市许可持有人
Interdos Pharma B.V
参考成员国 - 产品名称
Portugal (PT)
互认成员国 - 产品名称
United Kingdom (Northern Ireland) (XI)
Greece (GR)
许可日期
2019/08/14
最近更新日期
2024/04/19
药物ATC编码
M01AH04 parecoxib
申请类型
TypeLevel1:
Abridged
TypeLevel2:
Initial Application
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
|
633762_633763_20230317_PAR_ALB
Date of last change:2024/02/06
Final Product Information
|
common-impack-without-diluent
Date of last change:2020/01/15
Final Product Information
|
common-impack-with-diluent
Date of last change:2020/01/15
Final Product Information
|
common-pl-with-diluent-clean
Date of last change:2020/01/15
Final Product Information
|
common-outer-with-diluent
Date of last change:2020/01/15
Final Product Information
|
common-outer-without-diluent
Date of last change:2020/01/15
Final Product Information
|
common-spc-clean-without-diluent
Date of last change:2020/01/15
Final Product Information
|
common-pl-without-diluent-clean
Date of last change:2020/01/15
Final Product Information
|
common-spc-clean-with-diluent
Date of last change:2020/01/15
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase