Veterinary Medicine Information website

Versican Plus L4 (--) - Suspension for injection

Ima dovoljenje za promet

Leptospira interrogans, serovar Icterohaemorrhagiae, strain MSLB 1089, Inactivated
Leptospira interrogans, serovar Canicola, strain MSLB 1090, Inactivated
Leptospira kirschneri, serovar Grippotyphosa, strain MSLB 1091, Inactivated
Leptospira interrogans, serovar Bratislava, strain MSLB 1088, Inactivated

Informacije o zdravilu

Ime zdravila:

Versican Plus L4 (--) - Suspension for injection

Učinkovina:

Na voljo samo v English
Na voljo samo v English
Na voljo samo v English
Na voljo samo v English

Ciljne živalske vrste:

Na voljo samo v Bulgarian Spanish Czech Danish German Estonian Greek English French Italian Latvian Lithuanian Hungarian Dutch Romanian Finnish Swedish Icelandic Norwegian

Pot uporabe:

Subkutana uporaba

Podatki o zdravilu

Učinkovina / Jakost:

Na voljo samo v English

1.51

Antibody microagglutination-lytic reaction

/

1.00

Viala
Na voljo samo v English

1.51

Antibody microagglutination-lytic reaction

/

1.00

Viala
Na voljo samo v English

1.40

Antibody microagglutination-lytic reaction

/

1.00

Viala
Na voljo samo v English

Presentation_strength:1:51 ALR Reference:Ph EUR 0447 Comments:Suspension Index:3

Farmacevtska oblika:

Suspenzija za injiciranje

Anatomsko-terapevtsko-kemična veterinarska oznaka klasifikacija zdravil, ki se uporabljajo v veterini (ATCvet):

QI07AB01

Pravni status za dobavo/izdajo zdravila:

Zdravilo, ki se izdaja na veterinarski recept

Status dovoljenja za promet z zdravilom:

Valid

Ima dovoljenje za promet v:

Na voljo samo v Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Na voljo samo v Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Na voljo samo v Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Na voljo samo v Spanish Czech German Estonian English French Croatian Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Na voljo samo v Spanish Czech German Estonian Greek English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Na voljo samo v Spanish Czech German Estonian English French Italian Latvian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Na voljo samo v Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Na voljo samo v Spanish German Estonian English French Italian Dutch Portuguese Slovak Finnish Swedish Icelandic Norwegian
Na voljo samo v Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Na voljo samo v Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Na voljo samo v Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Na voljo samo v Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Na voljo samo v Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Na voljo samo v Spanish German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Na voljo samo v Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Na voljo samo v Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Na voljo samo v Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Na voljo samo v Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Na voljo samo v Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Na voljo samo v Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Na voljo samo v Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Na voljo samo v Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Na voljo samo v Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Na voljo samo v Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Na voljo samo v Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Na voljo samo v Spanish Czech German Estonian English French Italian Lithuanian Dutch Portuguese Romanian Slovak Swedish Icelandic Norwegian
Na voljo samo v Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Na voljo samo v Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Na voljo samo v Spanish Czech German Estonian English French Croatian Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Na voljo samo v Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Na voljo samo v Estonian English French Lithuanian Portuguese Swedish Icelandic Norwegian

Na voljo v:

Belgium
Cyprus
Denmark
Greece
Ireland
Italy
Luxembourg
Netherlands
United Kingdom (Northern Ireland)

Opis ovojnine zdravila:

Na voljo samo v English
Na voljo samo v English

Dodatne informacije

Vrsta dovoljenja:

Na voljo samo v English French Croatian Italian Latvian Finnish Swedish Icelandic Norwegian

Pravna podlaga za izdajo dovoljenja za promet z zdravilom:

Na voljo samo v English Italian Latvian Norwegian

Imetnik dovoljenja za promet z zdravilom:

Zoetis Belgium SA

Datum dovoljenja za promet z zdravilom:

31/07/2014

Proizvodna mesta, odgovorna za sproščanje serij:

Bioveta a.s.

Pristojni organ:

European Commission

Številka dovoljenja za promet z zdravilom:

Ta podatek za to zdravilo ni na voljo.

Datum spremembe statusa dovoljenja za promet:

31/07/2014

Za poročila o domnevnih neželenih učinkih zdravil za uporabo v veterinaski medicini obiščite stran: www.adrreports.eu/vet

Dokumenti

Combined File of all Documents

slovenščina (PDF)

Objavljeno na dan: 5/03/2025

Drugi jeziki (24)

English (PDF)

Objavljeno na dan: 5/03/2025

German (PDF)

Objavljeno na dan: 5/03/2025

Spanish (PDF)

Objavljeno na dan: 5/03/2025

Greek (PDF)

Objavljeno na dan: 5/03/2025

Bulgarian (PDF)

Objavljeno na dan: 5/03/2025

Czech (PDF)

Objavljeno na dan: 5/03/2025

Estonian (PDF)

Objavljeno na dan: 5/03/2025

Danish (PDF)

Objavljeno na dan: 5/03/2025

French (PDF)

Objavljeno na dan: 5/03/2025

Icelandic (PDF)

Objavljeno na dan: 5/03/2025

Latvian (PDF)

Objavljeno na dan: 5/03/2025

Croatian (PDF)

Objavljeno na dan: 5/03/2025

Italian (PDF)

Objavljeno na dan: 5/03/2025

Finnish (PDF)

Objavljeno na dan: 5/03/2025

Hungarian (PDF)

Objavljeno na dan: 5/03/2025

Lithuanian (PDF)

Objavljeno na dan: 5/03/2025

Maltese (PDF)

Objavljeno na dan: 5/03/2025

Dutch (PDF)

Objavljeno na dan: 5/03/2025

Portuguese (PDF)

Objavljeno na dan: 5/03/2025

Slovak (PDF)

Objavljeno na dan: 5/03/2025

Norwegian (PDF)

Objavljeno na dan: 5/03/2025

Romanian (PDF)

Objavljeno na dan: 5/03/2025

Polish (PDF)

Objavljeno na dan: 5/03/2025

Swedish (PDF)

Objavljeno na dan: 5/03/2025

ema-puar-versican-plus-l4-v-3680-par-en.pdf

English (PDF)

Objavljeno na dan: 16/03/2023