LABIPITUIN, 10 IU/ML ενέσιμο διάλυμα για αγελάδες, φοράδες, προβατίνες, αίγες, σύες, θηλυκούς σκύλους και γάτες
LABIPITUIN, 10 IU/ML ενέσιμο διάλυμα για αγελάδες, φοράδες, προβατίνες, αίγες, σύες, θηλυκούς σκύλους και γάτες
Pooblaščeno
- OXYTOCIN SYNTHETIC
Identifikacija zdravila
Ime zdravila:
LABIPITUIN, 10 IU/ML ενέσιμο διάλυμα για αγελάδες, φοράδες, προβατίνες, αίγες, σύες, θηλυκούς σκύλους και γάτες
Učinkovina:
- Na voljo samo v English
Ciljne živalske vrste:
-
krava
-
psice
Pot uporabe:
-
Subkutana uporaba
Podatki o zdravilu
Učinkovina / Jakost:
-
Na voljo samo v English10.00international unit(s)1.00millilitre(s)
Farmacevtska oblika:
-
Raztopina za injiciranje
Withdrawal period by route of administration:
-
Intramuscular and intravenous use
- Horse (mare)
-
Meat and offal3day
-
Milk24hour
-
- krava
-
Meat and offal3day
-
Milk24hour
-
- Sheep (ewe)
-
Meat and offal3day
-
Milk24day
-
- Goat (adult female)
-
Meat and offal3day
-
Milk24hour
-
- Pig (female)
-
Meat and offal3day
-
- psice
-
Meat and offalno withdrawal periodΔεν εφαρμόζεται
-
- Cat
-
Meat and offalno withdrawal periodΔεν εφαρμόζεται
-
-
Subkutana uporaba
- Horse (mare)
-
Meat and offal3day
-
Milk24hour
-
- krava
-
Meat and offal3day
-
Milk24hour
-
- Sheep (ewe)
-
Meat and offal3day
-
Milk24hour
-
- Goat (adult female)
-
Meat and offal3day
-
Milk24hour
-
- Pig (female)
-
Meat and offal3day
-
- psice
-
Meat and offalno withdrawal periodΔεν εφαρμόζεται
-
- Cat
-
Meat and offalno withdrawal periodΔεν εφαρμόζεται
-
Anatomsko-terapevtsko-kemična veterinarska oznaka (ATCvet):
- QH01BB02
Pravni status za dobavo / izdajo zdravila:
-
Zdravilo, ki se izdaja na veterinarski recept
Status dovoljenja:
-
Valid
Dodatne informacije
Pravna podlaga za izdajo dovoljenja za promet z zdravilom:
- Na voljo samo v English
Imetnik dovoljenja za promet z zdravilom:
- Hellafarm S.A.
Marketing authorisation date:
Proizvodna mesta, odgovorna za sproščanje serij:
- Labiana Life Sciences S.A.
Pristojni organ:
- National Organization For Medicines
Številka dovoljenja :
- 95628/22-10-2021/K-0114701
Datum spremembe statusa dovoljenja:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Dokumenti
Povzetek glavnih značilnosti zdravila
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Greek (PDF)
Objavljeno na: 27/12/2023
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