Veterinary Medicines

LABIXXIN 100MG/ML SOLUTION FOR INJECTION FOR CATTLE, PIGS AND SHEEP

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Tulathromycin

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Identifikacija zdravila

Ime zdravila:

LABIXXIN 100MG/ML SOLUTION FOR INJECTION FOR CATTLE, PIGS AND SHEEP

Labixxin, 100 mg/mL, otopina za injekciju, za goveda, svinje i ovce

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
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
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

Withdrawal period by route of administration:

intramuskularna uporaba
- Pig
  - Meat and offal
    
    13
    
    day
- Sheep
  - Meat and offal
    
    16
    
    day
- Sheep
  - Milk
    
    no withdrawal period
    
    Not authorised for use in animals producing milk for human consumption. Do not use in pregnant animals, which are intended to produce milk for human consumption, within 2 months of expected parturition.
Subkutana uporaba
- govedo
  - Meat and offal
    
    22
    
    day
- govedo
  - Milk
    
    no withdrawal period
    
    Not authorised for use in animals producing milk for human consumption. Do not use in pregnant animals, which are intended to produce milk for human consumption, within 2 months of expected parturition.

Anatomsko-terapevtsko-kemična veterinarska oznaka (ATCvet):

QJ01FA94

Pravni status za dobavo / izdajo zdravila:

Zdravilo, ki se izdaja na veterinarski recept

Status dovoljenja:

Valid

Authorised in:

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

Opis ovojnine:

Na voljo samo v English
Na voljo samo v English
Na voljo samo v English
Na voljo samo v English
Na voljo samo v English
Na voljo samo v English
Na voljo samo v English
Na voljo samo v English

Dodatne informacije

Entitlement type:

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:

Labiana Life Sciences S.A.

Marketing authorisation date:

24/11/2023

Proizvodna mesta, odgovorna za sproščanje serij:

Labiana Life Sciences S.A.

Pristojni organ:

Ministry Of Agriculture Veterinary And Food Safety Directorate

Številka dovoljenja :

UP/I-322-05/23-01/775

Datum spremembe statusa dovoljenja:

24/11/2023

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/0423/001

Zadevne države članice:

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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