欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号
EE/H/0304/002
药品名称
MELOXICAM-RATIOPHARM 15 MG
活性成分
meloxicam 7.5 mg
剂型
Tablet
上市许可持有人
ratiopharm GmbH Graf-Arco-Strasse 3, D-89079 Ulm Germany
参考成员国 - 产品名称
Estonia (EE)
互认成员国 - 产品名称
Lithuania (LT)
Meloxicam-ratiopharm 15 mg tabletės
许可日期
2008/11/24
最近更新日期
2023/09/21
药物ATC编码
M01AC06 meloxicam
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 Labelling
|
Annex_4_Labelling_DK_1398_OP_15 mg_09_11_10_clean
Date of last change:2024/09/06
Final Labelling
|
Annex_4_Labelling_DK_1398_OP_15 mg_09_11_10_MARK
Date of last change:2024/09/06
Final Labelling
|
Annex_4_Labelling_DK_1398_OP_7 5 mg_09_11_10_clean
Date of last change:2024/09/06
Final Labelling
|
Annex_4_Labelling_DK_1398_OP_7 5 mg_09_11_10_MARK
Date of last change:2024/09/06
Final Product Information
|
DK_H_0788_001_002_IB_017 Meloxicam
Date of last change:2024/09/06
Final Product Information
|
DK_H_0789_001_002_IB_011 Xelocam
Date of last change:2024/09/06
Final Product Information
|
DK_H_1398_001_002_IB_005 Loxime
Date of last change:2024/09/06
Final PL
|
Loxime 7_5_15 mg_EN_PIL_DK_H_1398_08_05_17
Date of last change:2024/09/06
Final SPC
|
Loxime 7_5_15 mg_EN_SPC_DK_H_1398_08_05_17
Date of last change:2024/09/06
PubAR
|
parmod5_dk1398loxime_pdf
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase