Librela

Country: European Union

Language: Lithuanian

Source: EMA (European Medicines Agency)

Active ingredient:

bedinvetmab

Available from:

Zoetis Belgium

ATC code:

QN02B

INN (International Name):

bedinvetmab

Therapeutic group:

Šunys

Therapeutic area:

Analgetikai

Therapeutic indications:

For the alleviation of pain associated with osteoarthritis in dogs.

Product summary:

Revision: 1

Authorization status:

Įgaliotas

Authorization date:

2020-11-10

Patient Information leaflet

                                OFFICIAL ADDRESS
Domenico Scarlattilaan 6
●
1083 HS Amsterdam
●
The Netherlands
An agency of the European Union
ADDRESS FOR VISITS AND DELIVERIES
Refer to www.ema.europa.eu/how-to-find-us
SEND US A QUESTION
Go to
www.ema.europa.eu/contact
TELEPHONE
+31 (0)88 781
6000
© European Medicines Agency,
2023. Reproduction is authorised provided the source is acknowledged.
Naujausia informacija apie šį veterinarinį vaistą pateikiama
veterinarinių vaistų informacijos svetainėje.
                                
                                Read the complete document
                                
                            

Summary of Product characteristics

                                OFFICIAL ADDRESS
Domenico Scarlattilaan 6
●
1083 HS Amsterdam
●
The Netherlands
An agency of the European Union
ADDRESS FOR VISITS AND DELIVERIES
Refer to www.ema.europa.eu/how-to-find-us
SEND US A QUESTION
Go to
www.ema.europa.eu/contact
TELEPHONE
+31 (0)88 781
6000
© European Medicines Agency,
2023. Reproduction is authorised provided the source is acknowledged.
Naujausia informacija apie šį veterinarinį vaistą pateikiama
veterinarinių vaistų informacijos svetainėje.
                                
                                Read the complete document
                                
                            

Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 31-05-2024
Summary of Product characteristics Summary of Product characteristics Bulgarian 31-05-2024
Public Assessment Report Public Assessment Report Bulgarian 31-05-2024
Patient Information leaflet Patient Information leaflet Spanish 31-05-2024
Public Assessment Report Public Assessment Report Spanish 31-05-2024
Patient Information leaflet Patient Information leaflet Czech 31-05-2024
Public Assessment Report Public Assessment Report Czech 31-05-2024
Patient Information leaflet Patient Information leaflet Danish 31-05-2024
Public Assessment Report Public Assessment Report Danish 31-05-2024
Patient Information leaflet Patient Information leaflet German 31-05-2024
Public Assessment Report Public Assessment Report German 31-05-2024
Patient Information leaflet Patient Information leaflet Estonian 31-05-2024
Public Assessment Report Public Assessment Report Estonian 31-05-2024
Patient Information leaflet Patient Information leaflet Greek 31-05-2024
Public Assessment Report Public Assessment Report Greek 31-05-2024
Patient Information leaflet Patient Information leaflet English 31-05-2024
Public Assessment Report Public Assessment Report English 31-05-2024
Patient Information leaflet Patient Information leaflet French 31-05-2024
Public Assessment Report Public Assessment Report French 31-05-2024
Patient Information leaflet Patient Information leaflet Italian 31-05-2024
Public Assessment Report Public Assessment Report Italian 31-05-2024
Patient Information leaflet Patient Information leaflet Latvian 31-05-2024
Public Assessment Report Public Assessment Report Latvian 31-05-2024
Patient Information leaflet Patient Information leaflet Hungarian 31-05-2024
Summary of Product characteristics Summary of Product characteristics Hungarian 31-05-2024
Public Assessment Report Public Assessment Report Hungarian 31-05-2024
Patient Information leaflet Patient Information leaflet Maltese 31-05-2024
Public Assessment Report Public Assessment Report Maltese 31-05-2024
Patient Information leaflet Patient Information leaflet Dutch 31-05-2024
Public Assessment Report Public Assessment Report Dutch 31-05-2024
Patient Information leaflet Patient Information leaflet Polish 31-05-2024
Public Assessment Report Public Assessment Report Polish 31-05-2024
Patient Information leaflet Patient Information leaflet Portuguese 31-05-2024
Summary of Product characteristics Summary of Product characteristics Portuguese 31-05-2024
Public Assessment Report Public Assessment Report Portuguese 31-05-2024
Patient Information leaflet Patient Information leaflet Romanian 31-05-2024
Public Assessment Report Public Assessment Report Romanian 31-05-2024
Patient Information leaflet Patient Information leaflet Slovak 31-05-2024
Public Assessment Report Public Assessment Report Slovak 31-05-2024
Patient Information leaflet Patient Information leaflet Slovenian 31-05-2024
Summary of Product characteristics Summary of Product characteristics Slovenian 31-05-2024
Public Assessment Report Public Assessment Report Slovenian 31-05-2024
Patient Information leaflet Patient Information leaflet Finnish 31-05-2024
Public Assessment Report Public Assessment Report Finnish 31-05-2024
Patient Information leaflet Patient Information leaflet Swedish 31-05-2024
Public Assessment Report Public Assessment Report Swedish 31-05-2024
Patient Information leaflet Patient Information leaflet Norwegian 31-05-2024
Summary of Product characteristics Summary of Product characteristics Norwegian 31-05-2024
Public Assessment Report Public Assessment Report Norwegian 31-05-2024
Patient Information leaflet Patient Information leaflet Icelandic 31-05-2024
Summary of Product characteristics Summary of Product characteristics Icelandic 31-05-2024
Public Assessment Report Public Assessment Report Icelandic 31-05-2024
Patient Information leaflet Patient Information leaflet Croatian 31-05-2024
Public Assessment Report Public Assessment Report Croatian 31-05-2024
Patient Information leaflet Patient Information leaflet Irish 31-05-2024
Public Assessment Report Public Assessment Report Irish 31-05-2024

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