Veterinary Medicine Information website

ENROX 100 mg/ml peroralna raztopina

Ima dovoljenje za promet

Enrofloxacin

Informacije o zdravilu

Ime zdravila:

ENROX 100 mg/ml peroralna raztopina

Učinkovina:

Na voljo samo v English

Ciljne živalske vrste:

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

Pot uporabe:

Dajanje v vodo za pitje

Podatki o zdravilu

Učinkovina / Jakost:

Na voljo samo v English

100.00

milligram(s)

/

1.00

millilitre(s)

Farmacevtska oblika:

Peroralna raztopina

Karenca glede na pot uporabe:

Dajanje v vodo za pitje
- Turkey
  - Meat and offal
    
    13
    
    day
    
    n.a.
  - Eggs
    
    no withdrawal period
    
    Not for use in birds producing eggs for human consumption.
- brojler
  - Meat and offal
    
    7
    
    day
    
    n.a.
- Chicken (for reproduction)
  - Meat and offal
    
    7
    
    day
    
    n.a.
  - Eggs
    
    no withdrawal period
    
    Do not use in layer replacement birds within 2 weeks before the start of the laying period.
  - Eggs
    
    no withdrawal period
    
    Not for use in birds producing eggs for human consumption.
- Chicken (pullet)
  - Meat and offal
    
    7
    
    day
    
    n.a.
  - Eggs
    
    no withdrawal period
    
    Do not use in layer replacement birds within 2 weeks before the start of the laying period.
  - Eggs
    
    no withdrawal period
    
    Not for use in birds producing eggs for human consumption.

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

QJ01MA90

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:

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Pravna podlaga za izdajo dovoljenja za promet z zdravilom:

Na voljo samo v English Italian Latvian Norwegian

Imetnik dovoljenja za promet z zdravilom:

KRKA tovarna zdravil d.d. Novo mesto

Datum dovoljenja za promet z zdravilom:

4/09/2006

Proizvodna mesta, odgovorna za sproščanje serij:

KRKA tovarna zdravil d.d. Novo mesto

Pristojni organ:

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

Številka dovoljenja za promet z zdravilom:

MR/V/0111/001

Datum spremembe statusa dovoljenja za promet:

4/09/2006

Referenčna država članica:

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Številka postopka:

SI/V/0100/001

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

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: 29/08/2024

Drugi jeziki (1)

English (PDF)

Objavljeno na dan: 29/08/2024

Navodilo za uporabo

slovenščina (PDF)

Objavljeno na dan: 29/08/2024

Drugi jeziki (1)

English (PDF)

Objavljeno na dan: 29/08/2024

Označevanje

slovenščina (PDF)

Objavljeno na dan: 29/08/2024

Drugi jeziki (1)

English (PDF)

Objavljeno na dan: 29/08/2024

PuAR_Enrox 100 p-o solution.pdf

English (PDF)

Objavljeno na dan: 29/08/2024