欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
DK/H/0123/001
药品名称
Xefo
活性成分
Lornoxicam 4.0 mg
剂型
Film-coated tablet
上市许可持有人
Takeda Pharma A/S Dybendal Alle 10 DK-2630 Taastrup Denmark
参考成员国 - 产品名称
Denmark (DK)
Xefo
互认成员国 - 产品名称
Greece (GR)
Slovakia (SK)
Austria (AT)
Xefo 4 mg - Filmtabletten
Latvia (LV)
Hungary (HU)
Lithuania (LT)
xefo 4 mg plėvele dengtos tabletės
许可日期
1997/07/01
最近更新日期
2024/12/04
药物ATC编码
M01AC05 lornoxicam
申请类型
TypeLevel1:
Known Active Substance
TypeLevel2:
Initial Application
TypeLevel3:
Full Dossier Article 4.8 Di 65/65
TypeLevel4:
Chemical Substance
TypeLevel5:
Prescription Only
附件文件下载
Final Labelling
|
0123 common_interpack_4mg
Date of last change:2024/09/06
Final Labelling
|
0123 common_interpack_8mg
Date of last change:2024/09/06
Final Labelling
|
0123 common_interpack_8mg_rapid
Date of last change:2024/09/06
Final Labelling
|
0123 common_interpack_inj
Date of last change:2024/09/06
Final PL
|
Lornoxicam_4mg_common_pl_DK_H123_H137_ clean
Date of last change:2024/09/06
Final Product Information
|
Lornoxicam_4mg_common_spc_DK_H123_H137_ clean
Date of last change:2024/09/06
Final SPC
|
Lornoxicam_4mg_common_spc_DK_H123_H137_IIVar_ccds7_clean
Date of last change:2024/09/06
Final SPC
|
Lornoxicam_8mg_common_spc_DK_H123_H137_IIVar_ccds7_clean
Date of last change:2024/09/06
Final SPC
|
Lornoxicam_8mg_Inj_common_spc_DK_H123_H137_IIVar_ccds7_clean
Date of last change:2024/09/06
Final SPC
|
Lornoxicam_8mgrapid_common_spc_DK_H123_IIVar_ccds7_clea
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase