REHIDRAVIT
REHIDRAVIT
Pooblaščeno
- Caffeine
- Calcium chloride dihydrate
- Glucose monohydrate
- Inositol
- Magnesium chloride hexahydrate
- Nicotinamide
- Potassium chloride
- Pyridoxine hydrochloride
- Riboflavin
- Sodium acetate trihydrate
- Sodium chloride
Identifikacija zdravila
Ime zdravila:
REHIDRAVIT
Ciljne živalske vrste:
-
tele
Pot uporabe:
-
Subkutana uporaba
-
Intraperitonealna uporaba
-
Intravenska uporaba
Podatki o zdravilu
Učinkovina / Jakost:
-
Na voljo samo v English0.38milligram(s)1.00millilitre(s)
-
Na voljo samo v English0.99milligram(s)1.00millilitre(s)
-
Na voljo samo v English50.00milligram(s)1.00millilitre(s)
-
Na voljo samo v English0.50milligram(s)1.00millilitre(s)
-
Na voljo samo v English0.64milligram(s)1.00millilitre(s)
-
Na voljo samo v English0.10milligram(s)1.00millilitre(s)
-
Na voljo samo v English0.37milligram(s)1.00millilitre(s)
-
Na voljo samo v English0.50milligram(s)1.00millilitre(s)
-
Na voljo samo v English0.02milligram(s)1.00millilitre(s)
-
Na voljo samo v English5.00milligram(s)1.00millilitre(s)
-
Na voljo samo v English7.00milligram(s)1.00millilitre(s)
Farmacevtska oblika:
-
Raztopina za injiciranje
Withdrawal period by route of administration:
-
Subkutana uporaba
- Horse (colt)
-
Meat and offal0day
-
- tele
-
Meat and offal0day
-
- Sheep (lamb)
-
Meat and offal0day
-
- Pig (piglet)
-
Meat and offal0day
-
- Dog
- Cat
-
Intraperitonealna uporaba
- tele
-
Meat and offal0day
-
- Horse (colt)
-
Meat and offal0day
-
- Sheep (lamb)
-
Meat and offal0day
-
- Pig (piglet)
-
Meat and offal0day
-
- Dog
- Cat
-
Intravenska uporaba
- Horse (colt)
-
Meat and offal0day
-
- tele
-
Meat and offal0day
-
- Sheep (lamb)
-
Meat and offal0day
-
- Pig (piglet)
-
Meat and offal0day
-
- Dog
- Cat
Anatomsko-terapevtsko-kemična veterinarska oznaka (ATCvet):
- QB05BB02
Pravni status za dobavo / izdajo zdravila:
Ta podatek za to zdravilo ni na voljo.
Status dovoljenja:
-
Valid
Available in:
-
Romania
Dodatne informacije
Pravna podlaga za izdajo dovoljenja za promet z zdravilom:
- Na voljo samo v English
Imetnik dovoljenja za promet z zdravilom:
- Pasteur Filiala Filipesti S.A.
Marketing authorisation date:
Proizvodna mesta, odgovorna za sproščanje serij:
- Pasteur Filiala Filipesti S.A.
Pristojni organ:
- Institute For Control Of Biological Products And Veterinary Medicines
Številka dovoljenja :
- 170201
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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Romanian (PDF)
Objavljeno na: 26/05/2022
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