欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
DE/H/2389/001
药品名称
Naratriptan Migräne STADA 2,5 mg Filmtabletten
活性成分
naratriptan hydrochloride 2.78 mg
剂型
Film-coated tablet
上市许可持有人
STADA Consumer Health Deutschland GmbH Stadastrasse 2-18 61118 Bad Vilbel Germany
参考成员国 - 产品名称
Germany (DE)
互认成员国 - 产品名称
Romania (RO)
Nacralid 2,5 mg comprimate filmate
许可日期
2010/04/28
最近更新日期
2024/01/22
药物ATC编码
N02CC02 naratriptan
申请类型
TypeLevel1:
Abridged
TypeLevel2:
Multiple (Copy) Application
TypeLevel3:
Generic Art 10.1 and 10.2 Dir 2001/83/EC
TypeLevel4:
Chemical Substance
TypeLevel5:
Non Prescription (including OTC)
附件文件下载
Final Labelling
|
DE2387_Naratriptan_labipen_cl_20150326_renewal
Date of last change:2024/09/06
Final Labelling
|
DE2387_Naratriptan_labopen_cl_20150326_renewal
Date of last change:2024/09/06
Final PL
|
DE2387_Naratriptan_PIL_cl_20150326_renewal
Date of last change:2024/09/06
Final SPC
|
DE2387_Naratriptan_SmPC_cl_20150326_renewal
Date of last change:2024/09/06
Final Labelling
|
DE2388_Naratriptan_labipen_cl_20150326_renewal
Date of last change:2024/09/06
Final Labelling
|
DE2388_Naratriptan_labopen_cl_20150326_renewal
Date of last change:2024/09/06
Final PL
|
DE2388_Naratriptan_PL_cl_20150326_renewal
Date of last change:2024/09/06
Final SPC
|
DE2388_Naratriptan_SmPC_cl_20150326_renewal
Date of last change:2024/09/06
Final Labelling
|
DE2389_Naratriptan_labipen_cl_20150326_renewal
Date of last change:2024/09/06
Final Labelling
|
DE2389_Naratriptan_labopen_cl_20150326_renewal
Date of last change:2024/09/06
Final PL
|
DE2389_Naratriptan_PL_cl_20150326_renewal
Date of last change:2024/09/06
Final SPC
|
DE2389_Naratriptan_SmPC_cl_20150326_renewal
Date of last change:2024/09/06
Final Labelling
|
DE2390_Naratriptan_labipen_cl_20150326_renewal
Date of last change:2024/09/06
Final Labelling
|
DE2390_Naratriptan_labopen_cl_20150326_renewal_doc
Date of last change:2024/09/06
Final PL
|
DE2390_Naratriptan_PL_cl_20150326_renewal
Date of last change:2024/09/06
Final SPC
|
DE2390_Naratriptan_SmPC_cl_20150326_renewal
Date of last change:2024/09/06
Final Product Information
|
final_common Labelling 2389_12
Date of last change:2024/09/06
Final Product Information
|
final_common PL 2389_12
Date of last change:2024/09/06
Final Product Information
|
final_common SPC 2389_12
Date of last change:2024/09/06
PubAR
|
PAREN_DE2387_2390_Naratriptan_20100527_final
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase