Veterinary Medicine Information website

Elivec 5 mg/ml kožni poliv, raztopina za govedo, ovce in koze

Ima dovoljenje za promet

Eprinomectin

Informacije o zdravilu

Ime zdravila:

Elivec 5 mg/ml kožni poliv, raztopina za govedo, ovce in koze

Učinkovina:

Na voljo samo v English

Ciljne živalske vrste:

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

Dermalna uporaba

Podatki o zdravilu

Učinkovina / Jakost:

Na voljo samo v English

5.00

milligram(s)

/

1.00

millilitre(s)

Farmacevtska oblika:

Kožni poliv, raztopina

Karenca glede na pot uporabe:

Dermalna uporaba
- govedo
  - Meat and offal
    
    15
    
    day
  - Milk
    
    0
    
    day
- Sheep
  - Meat and offal
    
    2
    
    day
  - Milk
    
    0
    
    day
- Goat
  - Meat and offal
    
    1
    
    day
  - Milk
    
    0
    
    day

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

QP54AA04

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:

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Na voljo v:

Slovenia

Opis ovojnine zdravila:

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 Norwegian

Imetnik dovoljenja za promet z zdravilom:

Industrial Veterinaria S.A.

Datum dovoljenja za promet z zdravilom:

4/06/2018

Proizvodna mesta, odgovorna za sproščanje serij:

aniMedica GmbH
Industrial Veterinaria S.A.
aniMedica Herstellungs GmbH

Pristojni organ:

Agency For Medicinal Products And Medical Devices Of The Republic Of Slovenia

Številka dovoljenja za promet z zdravilom:

DC/V/0626/001

Datum spremembe statusa dovoljenja za promet:

4/06/2018

Referenčna država članica:

Na voljo samo v Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian

Številka postopka:

FR/V/0313/001

Zadevne države članice:

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 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 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 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 Estonian English French Lithuanian Portuguese Swedish Icelandic Norwegian

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

Dokumenti

Povzetek glavnih značilnosti zdravila

slovenščina (PDF)

Objavljeno na dan: 30/01/2026

Navodilo za uporabo

slovenščina (PDF)

Objavljeno na dan: 30/01/2026

Označevanje

slovenščina (PDF)

Objavljeno na dan: 30/01/2026

Combined File of all Documents

Ta dokument ne obstaja v tem jeziku (slovenščina). Lahko ga najdete spodaj v drugem jeziku.

Drugi jeziki (1)

English (PDF)

Objavljeno na dan: 23/10/2025

Updated on: 13/03/2026

eu-puar-frv0313001-mr-rpe363-en.pdf

English (PDF)

Objavljeno na dan: 13/03/2026