LABIXXIN 100MG/ML SOLUTION FOR INJECTION FOR CATTLE, PIGS AND SHEEP
LABIXXIN 100MG/ML SOLUTION FOR INJECTION FOR CATTLE, PIGS AND SHEEP
Pooblaščeno
- Tulathromycin
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:
-
govedo
Pot uporabe:
-
intramuskularna uporaba
-
Subkutana uporaba
Podatki o zdravilu
Učinkovina / Jakost:
-
Na voljo samo v English100.00milligram(s)/millilitre1.00millilitre(s)
Farmacevtska oblika:
-
Raztopina za injiciranje
Withdrawal period by route of administration:
-
intramuskularna uporaba
- Pig
-
Meat and offal13day
-
- govedo
-
Meat and offal22day
-
Milkno withdrawal periodNot 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.
-
- Sheep
-
Meat and offal16day
-
Milkno withdrawal periodNot 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
- Pig
-
Meat and offal13day
-
- govedo
-
Meat and offal22day
-
Milkno withdrawal periodNot 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.
-
- Sheep
-
Meat and offal16day
-
Milkno withdrawal periodNot 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
Dodatne informacije
Imetnik dovoljenja za promet z zdravilom:
- Labiana Life Sciences S.A.
Marketing authorisation date:
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:
Številka postopka:
- ES/V/0423/001
Ta podatek za to zdravilo ni na voljo.
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Dokumenti
Povzetek glavnih značilnosti zdravila
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Croatian (PDF)
Objavljeno na: 5/01/2024
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