ALFADEXX 2 MG/ML SOLUTION FOR INJECTION FOR HORSES, CATTLE, GOATS, PIGS, DOGS AND CATS
ALFADEXX 2 MG/ML SOLUTION FOR INJECTION FOR HORSES, CATTLE, GOATS, PIGS, DOGS AND CATS
Pooblaščeno
- DEXAMETHASONE DISODIUM PHOSPHATE
Identifikacija zdravila
Ime zdravila:
ALFADEXX 2 MG/ML SOLUTION FOR INJECTION FOR HORSES, CATTLE, GOATS, PIGS, DOGS AND CATS
Alfadexx 2 mg/ml injekčný roztok pre kone, hovädzí dobytok, kozy, ošípané, psy a mačky
Učinkovina:
- Na voljo samo v English
Ciljne živalske vrste:
-
govedo
Pot uporabe:
-
intramuskularna uporaba
-
Subkutana uporaba
-
Periartikularna uporaba
-
Intravenska uporaba
-
Intraartikularna uporaba
Podatki o zdravilu
Učinkovina / Jakost:
-
Na voljo samo v English2.63milligram(s)1.00millilitre(s)
Farmacevtska oblika:
-
Raztopina za injiciranje
Withdrawal period by route of administration:
-
intramuskularna uporaba
- govedo
-
Meat and offal8day
-
Milk72hour
-
- Pig
-
Meat and offal2day
-
- Cat
- Horse
-
Meat and offal8day
-
Milkno withdrawal periodNo withdrawal period
-
- Goat
-
Meat and offal8day
-
Milk72hour
-
- Dog
-
Subkutana uporaba
- Dog
- Cat
-
Periartikularna uporaba
- Horse
-
Meat and offal8day
-
Milkno withdrawal periodNo withdrawal period
-
-
Intravenska uporaba
- govedo
-
Meat and offal8day
-
Milk72hour
-
- Pig
-
Meat and offal6day
-
- Cat
- Horse
-
Meat and offal8day
-
Milkno withdrawal periodNo withdrawal period
-
- Goat
-
Meat and offal8day
-
Milk72hour
-
- Dog
-
Intraartikularna uporaba
- Horse
-
Meat and offal8day
-
Milkno withdrawal periodNo withdrawal period
-
Anatomsko-terapevtsko-kemična veterinarska oznaka (ATCvet):
- QH02AB02
Pravni status za dobavo / izdajo zdravila:
-
Zdravilo, ki se izdaja na veterinarski recept
Status dovoljenja:
-
Valid
Dodatne informacije
Imetnik dovoljenja za promet z zdravilom:
- Alfasan Nederland B.V.
Marketing authorisation date:
Proizvodna mesta, odgovorna za sproščanje serij:
- Produlab Pharma B.V.
- Alfasan Nederland B.V.
Pristojni organ:
- Institute For State Control Of Veterinary Biologicals And Medicaments
Številka dovoljenja :
- 96/031/DC/21-S
Datum spremembe statusa dovoljenja:
Številka postopka:
- FR/V/0430/001
Zadevne države članice:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Dokumenti
Combined File of all Documents
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Slovak (PDF)
Objavljeno na: 19/03/2024
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