Veterinary Medicine Information website

Evant (--) - Suspension and solution for oral spray

Ima dovoljenje za promet

Eimeria acervulina, strain 003, Live
Eimeria maxima, strain 013, Live
Eimeria mitis, strain 006, Live
Eimeria praecox, strain 007, Live
Eimeria tenella, strain 004, Live

Informacije o zdravilu

Ime zdravila:

Evant (--) - Suspension and solution for oral spray

Učinkovina:

Na voljo samo v English
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:

Peroralna uporaba

Podatki o zdravilu

Učinkovina / Jakost:

Na voljo samo v English

Presentation_strength:332-450 sporulated oocysts Reference:Ph. Eur. Index:0
Na voljo samo v English

Presentation_strength:196-265 sporulated oocysts Reference:Ph. Eur. Index:1
Na voljo samo v English

Presentation_strength:293-397 sporulated oocysts Reference:Ph. Eur. Index:2
Na voljo samo v English

Presentation_strength:293-397 sporulated oocysts Reference:Ph. Eur. Index:3
Na voljo samo v English

Presentation_strength:276-374 sporulated oocysts Reference:Ph. Eur. Index:4

Farmacevtska oblika:

Ta podatek za to zdravilo ni na voljo.

Karenca glede na pot uporabe:

Peroralna uporaba
- Chicken
  - Not applicable
    
    0
    
    day
    
    Zero days

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

QI01AN01

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

Opis ovojnine zdravila:

Na voljo samo v English
Na voljo samo v English
Na voljo samo v English
Na voljo samo v English
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 Lithuanian Norwegian

Imetnik dovoljenja za promet z zdravilom:

Laboratorios Hipra S.A.

Datum dovoljenja za promet z zdravilom:

5/02/2019

Proizvodna mesta, odgovorna za sproščanje serij:

Laboratorios Hipra S.A.

Pristojni organ:

European Commission

Številka dovoljenja za promet z zdravilom:

Ta podatek za to zdravilo ni na voljo.

Datum spremembe statusa dovoljenja za promet:

5/02/2019

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: 14/03/2026

Drugi jeziki (24)

English (PDF)

Objavljeno na dan: 14/03/2026

Czech (PDF)

Objavljeno na dan: 14/03/2026

Danish (PDF)

Objavljeno na dan: 14/03/2026

German (PDF)

Objavljeno na dan: 14/03/2026

Greek (PDF)

Objavljeno na dan: 14/03/2026

Bulgarian (PDF)

Objavljeno na dan: 14/03/2026

Spanish (PDF)

Objavljeno na dan: 14/03/2026

Estonian (PDF)

Objavljeno na dan: 14/03/2026

Finnish (PDF)

Objavljeno na dan: 14/03/2026

French (PDF)

Objavljeno na dan: 14/03/2026

Croatian (PDF)

Objavljeno na dan: 14/03/2026

Hungarian (PDF)

Objavljeno na dan: 14/03/2026

Icelandic (PDF)

Objavljeno na dan: 14/03/2026

Italian (PDF)

Objavljeno na dan: 14/03/2026

Lithuanian (PDF)

Objavljeno na dan: 14/03/2026

Latvian (PDF)

Objavljeno na dan: 14/03/2026

Maltese (PDF)

Objavljeno na dan: 14/03/2026

Dutch (PDF)

Objavljeno na dan: 14/03/2026

Norwegian (PDF)

Objavljeno na dan: 14/03/2026

Polish (PDF)

Objavljeno na dan: 14/03/2026

Portuguese (PDF)

Objavljeno na dan: 14/03/2026

Romanian (PDF)

Objavljeno na dan: 14/03/2026

Slovak (PDF)

Objavljeno na dan: 14/03/2026

Swedish (PDF)

Objavljeno na dan: 14/03/2026

ema-puar-evant-v-4902-par-en.pdf

English (PDF)

Objavljeno na dan: 14/03/2026