Gumbohatch

Country: European Union

Language: Norwegian

Source: EMA (European Medicines Agency)

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Active ingredient:

levende svekket smittsomme bursal disease virus (IBDV), belastning 1052

Available from:

Laboratorios Hipra, S.A.

ATC code:

QI01AD09

INN (International Name):

avian infectious bursal disease vaccine (live)

Therapeutic group:

Chicken; Embryonated chicken eggs

Therapeutic area:

Immunologicals for aves, Innenlandske fugler, Live viral vaksiner, avian smittsomme bursal disease virus (gumboro sykdom)

Therapeutic indications:

For aktive vaksinering av 1-dag-gamle broiler unger og embryonated broiler kylling egg for å redusere kliniske tegn og lesjoner i bursa av Fabricius forårsaket av svært virulente avian smittsomme bursal sykdom virus infeksjon.

Product summary:

Revision: 2

Authorization status:

autorisert

Authorization date:

2019-11-12

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.
Oppdaterte opplysninger om dette legemidlet til dyr er tilgjengelige
på informasjonsnettstedet for
legemidler til dyr.
                                
                                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.
Oppdaterte opplysninger om dette legemidlet til dyr er tilgjengelige
på informasjonsnettstedet for
legemidler til dyr.
                                
                                Read the complete document
                                
                            

Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 15-02-2024
Summary of Product characteristics Summary of Product characteristics Bulgarian 15-02-2024
Public Assessment Report Public Assessment Report Bulgarian 15-02-2024
Patient Information leaflet Patient Information leaflet Spanish 15-02-2024
Public Assessment Report Public Assessment Report Spanish 15-02-2024
Patient Information leaflet Patient Information leaflet Czech 15-02-2024
Public Assessment Report Public Assessment Report Czech 15-02-2024
Patient Information leaflet Patient Information leaflet Danish 15-02-2024
Public Assessment Report Public Assessment Report Danish 15-02-2024
Patient Information leaflet Patient Information leaflet German 15-02-2024
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Patient Information leaflet Patient Information leaflet Estonian 15-02-2024
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Public Assessment Report Public Assessment Report Latvian 15-02-2024
Patient Information leaflet Patient Information leaflet Lithuanian 15-02-2024
Summary of Product characteristics Summary of Product characteristics Lithuanian 15-02-2024
Public Assessment Report Public Assessment Report Lithuanian 15-02-2024
Patient Information leaflet Patient Information leaflet Hungarian 15-02-2024
Summary of Product characteristics Summary of Product characteristics Hungarian 15-02-2024
Public Assessment Report Public Assessment Report Hungarian 15-02-2024
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Patient Information leaflet Patient Information leaflet Dutch 15-02-2024
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Patient Information leaflet Patient Information leaflet Polish 15-02-2024
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Patient Information leaflet Patient Information leaflet Portuguese 15-02-2024
Summary of Product characteristics Summary of Product characteristics Portuguese 15-02-2024
Public Assessment Report Public Assessment Report Portuguese 15-02-2024
Patient Information leaflet Patient Information leaflet Romanian 15-02-2024
Public Assessment Report Public Assessment Report Romanian 15-02-2024
Patient Information leaflet Patient Information leaflet Slovak 15-02-2024
Public Assessment Report Public Assessment Report Slovak 15-02-2024
Patient Information leaflet Patient Information leaflet Slovenian 15-02-2024
Summary of Product characteristics Summary of Product characteristics Slovenian 15-02-2024
Public Assessment Report Public Assessment Report Slovenian 15-02-2024
Patient Information leaflet Patient Information leaflet Finnish 15-02-2024
Public Assessment Report Public Assessment Report Finnish 15-02-2024
Patient Information leaflet Patient Information leaflet Swedish 15-02-2024
Public Assessment Report Public Assessment Report Swedish 15-02-2024
Patient Information leaflet Patient Information leaflet Icelandic 15-02-2024
Summary of Product characteristics Summary of Product characteristics Icelandic 15-02-2024
Public Assessment Report Public Assessment Report Icelandic 15-02-2024
Patient Information leaflet Patient Information leaflet Croatian 15-02-2024
Public Assessment Report Public Assessment Report Croatian 15-02-2024
Patient Information leaflet Patient Information leaflet Irish 15-02-2024
Public Assessment Report Public Assessment Report Irish 15-02-2024

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