Veterinary Medicine Information website

VETIPRACIN 250 IU/MG POWDER FOR USE IN DRINKING WATER/MILK REPLACER

Ima dovoljenje za promet

Apramycin sulfate

Informacije o zdravilu

Ime zdravila:

VETIPRACIN 250 IU/MG POWDER FOR USE IN DRINKING WATER/MILK REPLACER

Učinkovina:

Na voljo samo v English

Ciljne živalske vrste:

brojler
Na voljo samo v Bulgarian Spanish Czech Danish 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 English French Italian Latvian Lithuanian Hungarian Dutch Romanian Finnish Swedish Norwegian

Pot uporabe:

Dajanje v vodo za pitje/mleko

Podatki o zdravilu

Učinkovina / Jakost:

Na voljo samo v English

250000.00

international unit(s)/gram

/

1.00

gram(s)

Farmacevtska oblika:

Prašek za dajanje v vodo za pitje/mleko

Karenca glede na pot uporabe:

Dajanje v vodo za pitje/mleko
- brojler
  - Meat and offal
    
    0
    
    day
- Rabbit
  - Meat and offal
    
    0
    
    day
- Pig (weaned piglet)
  - Meat and offal
    
    0
    
    day
- Cattle (pre-ruminant)
  - Meat and offal
    
    28
    
    day
- brojler
  - Eggs
    
    no withdrawal period
    
    Not for use in birds producing or intended to produce eggs for human consumption. Do not use within 4 weeks before the start of the laying period.

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

QA07AA92

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 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 French Italian Latvian Lithuanian Norwegian

Imetnik dovoljenja za promet z zdravilom:

Laboratorios Maymo S.A.U.

Datum dovoljenja za promet z zdravilom:

10/04/2025

Proizvodna mesta, odgovorna za sproščanje serij:

Laboratorios Maymo S.A.U.

Pristojni organ:

Danish Medicines Agency

Številka dovoljenja za promet z zdravilom:

71392

Datum spremembe statusa dovoljenja za promet:

10/04/2025

Referenčna država članica:

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

Številka postopka:

ES/V/0442/001

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 English French Italian Dutch Portuguese Slovak 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

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

Drugi jeziki (1)

English (PDF)

Objavljeno na dan: 5/06/2025

Navodilo za uporabo

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

Drugi jeziki (1)

English (PDF)

Objavljeno na dan: 5/06/2025

eu-PUAR-esv0442001-dcp-vetipracin-250-iu-mg-powder-for-use-in-drinking-water-milk-replacer-en.pdf

English (PDF)

Objavljeno na dan: 24/07/2025