FOSFOCARNITINA
FOSFOCARNITINA
Pooblaščeno
- DL-methionine
- L-ASPARTIC ACID
- Cyanocobalamin
- Lysine hydrochloride
- L-arginine hydrochloride
- L-THREONINE
- Phosphorylcolamine
- Propyl parahydroxybenzoate
- ACETYLCARNITINE
Identifikacija zdravila
Ime zdravila:
FOSFOCARNITINA
Ciljne živalske vrste:
-
govedo
Pot uporabe:
-
intramuskularna uporaba
-
Intravenska uporaba
-
Subkutana uporaba
Podatki o zdravilu
Učinkovina / Jakost:
-
Na voljo samo v English1.50gram(s)100.00millilitre(s)
-
Na voljo samo v English2.70gram(s)100.00millilitre(s)
-
Na voljo samo v English10.00milligram(s)100.00millilitre(s)
-
Na voljo samo v English3.00gram(s)100.00millilitre(s)
-
Na voljo samo v English1.20gram(s)100.00millilitre(s)
-
Na voljo samo v English1.00gram(s)100.00millilitre(s)
-
Na voljo samo v English6.00gram(s)100.00millilitre(s)
-
Na voljo samo v English0.02gram(s)100.00millilitre(s)
-
Na voljo samo v English1.00gram(s)100.00millilitre(s)
Farmacevtska oblika:
-
Raztopina za injiciranje
Withdrawal period by route of administration:
-
intramuskularna uporaba
- Buffalo
-
Milk0day
-
Meat and offal0day
-
- govedo
-
Milk0day
-
Meat and offal0day
-
- Goat
-
Milk0day
-
Meat and offal0day
-
- Sheep
-
Milk0day
-
Meat and offal0day
-
- Pig
-
Meat and offal0day
-
- Horse
-
Meat and offal0day
-
-
Intravenska uporaba
- govedo
-
Milk0day
-
Meat and offal0day
-
- Goat
-
Milk0day
-
Meat and offal0day
-
- Sheep
-
Milk0day
-
Meat and offal0day
-
- Horse
-
Meat and offal0day
-
-
Subkutana uporaba
- Goat
-
Milk0day
-
Meat and offal0day
-
- Sheep
-
Milk0day
-
Meat and offal0day
-
- Rabbit
-
Meat and offal0day
-
Anatomsko-terapevtsko-kemična veterinarska oznaka (ATCvet):
- QA16AA51
Pravni status za dobavo / izdajo zdravila:
-
Zdravilo, ki se izdaja brez veterinarskega recepta
Status dovoljenja:
-
Valid
Dodatne informacije
Imetnik dovoljenja za promet z zdravilom:
- Zoetis Italia S.r.l
Marketing authorisation date:
Proizvodna mesta, odgovorna za sproščanje serij:
- Zoetis Manufacturing & Research Spain S.L.
Pristojni organ:
- Ministry Of Health
Številka dovoljenja :
Ta podatek za to zdravilo ni na voljo.
Datum spremembe statusa dovoljenja:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Dokumenti
Combined File of all Documents
Ta dokument ne obstaja v tem jeziku (slovenščina). Spodaj ga najdete v drugem jeziku.
Italian (PDF)
Objavljeno na: 2/03/2023
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