INTROVIT-E-SELEN, injekcinis tirpalas veršeliams, ožkoms, avims ir kiaulėms

Ima dovoljenje za promet

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Informacije o zdravilu

Ime zdravila:

INTROVIT-E-SELEN, injekcinis tirpalas veršeliams, ožkoms, avims ir kiaulėms

Učinkovina:

Na voljo samo v English
Na voljo samo v English

Ciljne živalske vrste:

tele
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
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:

intramuskularna uporaba
Subkutana uporaba

Podatki o zdravilu

Učinkovina / Jakost:

Na voljo samo v English

0.50

milligram(s)

/

1.00

millilitre(s)
Na voljo samo v English

50.00

milligram(s)

/

1.00

millilitre(s)

Farmacevtska oblika:

Raztopina za injiciranje

Karenca glede na pot uporabe:

intramuskularna uporaba
- Goat
  - Milk
    
    no withdrawal period
    
    Not authorized for use in females, whose milk is meant for human consumption.
- Sheep
  - Milk
    
    no withdrawal period
    
    Not authorized for use in females, whose milk is meant for human consumption.
Subkutana uporaba
- Goat
  - Milk
    
    no withdrawal period
    
    Not authorized for use in females, whose milk is meant for human consumption.
- Sheep
  - Milk
    
    no withdrawal period
    
    Not authorized for use in females, whose milk is meant for human consumption.

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

QA11AA04

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

Opis ovojnine zdravila:

Na voljo samo v Lithuanian
Na voljo samo v Lithuanian

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 French Italian Latvian Norwegian

Imetnik dovoljenja za promet z zdravilom:

Interchemie werken De Adelaar LT UAB

Datum dovoljenja za promet z zdravilom:

2/11/2014

Proizvodna mesta, odgovorna za sproščanje serij:

Interchemie Werken De Adelaar Eesti AS

Pristojni organ:

State Food And Veterinary Service

Številka dovoljenja za promet z zdravilom:

LT/2/14/2258/001-002

Datum spremembe statusa dovoljenja za promet:

27/10/2025

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

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