Memantine LEK

ประเทศ: สหภาพยุโรป

ภาษา: ลิทัวเนีย

แหล่งที่มา: EMA (European Medicines Agency)

สารออกฤทธิ์:

Memantino hidrochloridas

มีจำหน่ายจาก:

Pharmathen S.A.

รหัส ATC:

N06DX01

INN (ชื่อสากล):

memantine

กลุ่มบำบัด:

Psychoanaleptics, , Kitos stabdžių-demencija narkotikų

พื้นที่บำบัด:

Alzhaimerio liga

ข้อบ่งชี้ในการรักษา:

Gydymas pacientams, sergantiems vidutinio sunkumo ar sunkia Alzhaimerio liga.

สรุปสินค้า:

Revision: 5

สถานะการอนุญาต:

Įgaliotas

วันที่อนุญาต:

2013-04-21

แผ่นพับข้อมูลผู้ป่วย

Skip to main content [European Medicines Agency]
Menu *
EMA WEBSITE TEMPORARILY UNAVAILABLE
This website is currently unavailable due to essential maintenance.
EMERGENCY CONTACT DETAILS
To report a potentially serious problem with a centrally authorised
medicine, call our product emergency hotline on [phone].
To report a product quality defect, including a suspected defect, of a
centrally authorised medicine that could result in a recall or
abnormal restriction on supply, marketing or manufacturing
authorisation holders can call [phone] outside business
hours.
The details of your call may be documented, including personal data if
you provide them (such as your name, contact details and nature of the
issue raised), in accordance with our privacy statement. You can
consult our privacy statement at
https://www.ema.europa.eu/en/about-us/legal/general-privacy-statement
[/en/about-us/legal/general-privacy-statement] once the website is
back online.
RSS feed Twitter YouTube LinkedIn
© 1995-2020 European Medicines Agency
European Union agencies network [European Union agencies network]
An agency of the European Union [European Union flag]

สรุปลักษณะสินค้า

Skip to main content [European Medicines Agency]
Menu *
EMA WEBSITE TEMPORARILY UNAVAILABLE
This website is currently unavailable due to essential maintenance.
EMERGENCY CONTACT DETAILS
To report a potentially serious problem with a centrally authorised
medicine, call our product emergency hotline on [phone].
To report a product quality defect, including a suspected defect, of a
centrally authorised medicine that could result in a recall or
abnormal restriction on supply, marketing or manufacturing
authorisation holders can call [phone] outside business
hours.
The details of your call may be documented, including personal data if
you provide them (such as your name, contact details and nature of the
issue raised), in accordance with our privacy statement. You can
consult our privacy statement at
https://www.ema.europa.eu/en/about-us/legal/general-privacy-statement
[/en/about-us/legal/general-privacy-statement] once the website is
back online.
RSS feed Twitter YouTube LinkedIn
© 1995-2020 European Medicines Agency
European Union agencies network [European Union agencies network]
An agency of the European Union [European Union flag]