Baytril One 100 mg/ml Injektionslösung für Rinder und Schweine

Ima dovoljenje za promet

Enrofloxacin

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Informacije o zdravilu

Ime zdravila:

Baytril One 100 mg/ml Injektionslösung für Rinder und Schweine

BAYTRIL One 100 mg/ml injekčný roztok pre hovädzí dobytok a ošípané

Učinkovina:

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
govedo

Pot uporabe:

intramuskularna uporaba
Intravenska uporaba
Subkutana uporaba

Podatki o zdravilu

Učinkovina / Jakost:

Na voljo samo v English

100.00

milligram(s)

/

1.00

millilitre(s)

Farmacevtska oblika:

Raztopina za injiciranje

Karenca glede na pot uporabe:

intramuskularna uporaba
- Pig
  - Meat and offal
    
    12
    
    day
    
    7,5 mg/kg KGW/Tag, ev 2. Injektion in Abstand von 48 Std.
Intravenska uporaba
- govedo
  - Meat and offal
    
    7
    
    day
    
    5 mg/kg KGW/Tag für 2-3 Tage
  - Milk
    
    72
    
    hour
    
    5 mg/kg KGW/Tag für 2-3 Tage
Subkutana uporaba
- govedo
  - Meat and offal
    
    14
    
    day
    
    7,5 mg/kg KGW/Tag, ev. 2. Injektion in Abstand von 48 Std.
  - Milk
    
    120
    
    hour
    
    7,5 mg/kg KGW/Tag, ev. 2. Injektion in Abstand von 48 Std.

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:

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 Italian Latvian Norwegian

Imetnik dovoljenja za promet z zdravilom:

Elanco Animal Health GmbH

Datum dovoljenja za promet z zdravilom:

20/12/2017

Proizvodna mesta, odgovorna za sproščanje serij:

KVP Pharma+Veterinaer Produkte GmbH

Pristojni organ:

Institute For State Control Of Veterinary Biologicals And Medicaments

Številka dovoljenja za promet z zdravilom:

96/058/MR/17-S

Datum spremembe statusa dovoljenja za promet:

20/12/2017

Referenčna država članica:

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

Številka postopka:

AT/V/0001/001

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 Croatian 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 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 Croatian 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

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