VETRISULF, milteliai geriamajam tirpalui

Ima dovoljenje za promet

Trimethoprim
Sulfaclozine sodium

Prenes kot PDF

Informacije o zdravilu

Ime zdravila:

VETRISULF, milteliai geriamajam tirpalui

Učinkovina:

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
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 Norwegian

Pot uporabe:

Dajanje v vodo za pitje

Podatki o zdravilu

Učinkovina / Jakost:

Na voljo samo v English

0.10

gram(s)

/

1.00

gram(s)
Na voljo samo v English

0.50

gram(s)

/

1.00

gram(s)

Farmacevtska oblika:

Prašek za peroralno raztopino

Karenca glede na pot uporabe:

Dajanje v vodo za pitje
- Chicken
  - Meat
    
    3
    
    day
  - Egg
    
    no withdrawal period
    
    Not authorized for use in birds, whose eggs are meant for human consumption.
- Turkey
  - Meat
    
    3
    
    day
  - Egg
    
    no withdrawal period
    
    Not authorized for use in birds, whose eggs are meant for human consumption.
- Goose
  - Meat
    
    3
    
    day
  - Egg
    
    no withdrawal period
    
    Not authorized for use in birds, whose eggs are meant for human consumption.

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

QJ01EW12

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
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:

Lavet Kft.

Datum dovoljenja za promet z zdravilom:

5/04/2007

Proizvodna mesta, odgovorna za sproščanje serij:

Lavet Kft.

Pristojni organ:

State Food And Veterinary Service

Številka dovoljenja za promet z zdravilom:

LT/2/07/1742/001-003

Datum spremembe statusa dovoljenja za promet:

26/04/2012

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

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