欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
PT/H/1662/001
药品名称
Ropivacaína Aurovitas
活性成分
ropivacaine hydrochloride 2.0 mg/ml
剂型
Solution for injection
上市许可持有人
Generis Farmacêutica, S.A.
参考成员国 - 产品名称
Portugal (PT)
互认成员国 - 产品名称
许可日期
2010/07/12
最近更新日期
2024/01/22
药物ATC编码
N01BB09 ropivacaine
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 PL
|
common_pl_proposedclean_2mgml_7_5mgml_10mgml
Date of last change:2024/09/06
Final SPC
|
common_spc_proposedclean_2mgml_7_5mgml_10mgml
Date of last change:2024/09/06
Final Labelling
|
LAB_Ropivacaine_DE_H_2212_01_03_04_R01_CL_20121205_doc
Date of last change:2024/09/06
Final Labelling
|
LAB_Ropivacaine_DE_H_2212_2_R01_CL_20121205_doc
Date of last change:2024/09/06
Final Labelling
|
LAB_Ropivacaine_DE_H_2212_5_R01_CL_20121205_doc
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase