Covexin 10 Suspension for Injection for Sheep and Cattle
Covexin 10 Suspension for Injection for Sheep and Cattle
Pooblaščeno
- Clostridium haemolyticum, toxoid
- Clostridium sordellii, toxoid
- Tetanus toxoid adsorbed
- Clostridium septicum, toxoid
- Clostridium novyi, toxoid
- Clostridium perfringens, type D, epsilon toxoid
- Clostridium perfringens, type B and C, beta toxoid
- Clostridium chauvoei, Inactivated
- Clostridium perfringens, type A and C, alpha toxoid
Identifikacija zdravila
Ime zdravila:
Covexin 10 Suspension for injection for sheep and cattle
Covexin 10 Suspension for Injection for Sheep and Cattle
Pot uporabe:
-
Subkutana uporaba
Podatki o zdravilu
Učinkovina / Jakost:
-
Na voljo samo v English16.50enzyme-linked immunosorbent assay unit1.00millilitre(s)
-
Na voljo samo v English0.80enzyme-linked immunosorbent assay unit1.00millilitre(s)
-
Na voljo samo v English2.50enzyme-linked immunosorbent assay unit1.00millilitre(s)
-
Na voljo samo v English3.60enzyme-linked immunosorbent assay unit1.00millilitre(s)
-
Na voljo samo v English1.20enzyme-linked immunosorbent assay unit1.00millilitre(s)
-
Na voljo samo v English5.10enzyme-linked immunosorbent assay unit1.00millilitre(s)
-
Na voljo samo v English12.40enzyme-linked immunosorbent assay unit1.00millilitre(s)
-
Na voljo samo v English90.00percentage protection1.00millilitre(s)
-
Na voljo samo v English0.90enzyme-linked immunosorbent assay unit1.00millilitre(s)
Farmacevtska oblika:
-
Suspenzija za injiciranje
Withdrawal period by route of administration:
-
Subkutana uporaba
-
govedo
-
Milk0day
-
Meat and offal0day
-
-
Sheep
-
Meat and offal0day
-
Milk0day
-
-
Anatomsko-terapevtsko-kemična veterinarska oznaka (ATCvet):
- QI02AB01
- QI04AB01
Pravni status za dobavo / izdajo zdravila:
-
Zdravilo, ki se izdaja na veterinarski recept
Status dovoljenja:
-
Valid
Authorised in:
Available in:
-
United Kingdom (Northern Ireland)
Opis ovojnine:
- Na voljo samo v English
Dodatne informacije
Imetnik dovoljenja za promet z zdravilom:
- Zoetis UK Limited
Marketing authorisation date:
Proizvodna mesta, odgovorna za sproščanje serij:
- Zoetis Belgium
- Schering-Plough Limited
Pristojni organ:
- The Veterinary Medicines Directorate
Številka dovoljenja :
- Vm 42058/4022
Datum spremembe statusa dovoljenja:
Številka postopka:
- DE/V/0283/001
Zadevne države članice:
Za poročila o domnevnih neželenih učinkih zdravil za uporabo v veterinaski medicini obiščite stran: www.adrreports.eu/vet
Kako koristna je bila ta stran?: