Covexin 10 Suspension for injection for sheep and cattle
Covexin 10 Suspension for injection for sheep and cattle
Pooblaščeno
- Clostridium perfringens, type A, alpha toxoid
- 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
Identifikacija zdravila
Ime zdravila:
Covexin 10 Suspension for injection for sheep and cattle
Covexin 10, ενέσιμο εναιώρημα για πρόβατα και βοοειδή
Pot uporabe:
-
Subkutana uporaba
Podatki o zdravilu
Učinkovina / Jakost:
-
Na voljo samo v English0.90enzyme-linked immunosorbent assay unit1.00millilitre(s)
-
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)
Farmacevtska oblika:
-
Suspenzija za injiciranje
Withdrawal period by route of administration:
-
Subkutana uporaba
- govedo
-
Meat and offal0day
-
Milk0day
-
- 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
Dodatne informacije
Imetnik dovoljenja za promet z zdravilom:
- Zoetis Hellas S.A.
Marketing authorisation date:
Proizvodna mesta, odgovorna za sproščanje serij:
- Zoetis Belgium
- Schering-Plough Limited
Pristojni organ:
- Veterinary Services, Ministry Of Agriculture, Natural Resources And Environment
Številka dovoljenja :
- CY00218V
Datum spremembe statusa dovoljenja:
Številka postopka:
- DE/V/0283/001
Zadevne države članice:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Dokumenti
Povzetek glavnih značilnosti zdravila
Ta dokument ne obstaja v tem jeziku (slovenščina). Spodaj ga najdete v drugem jeziku.
English (PDF)
Objavljeno na: 4/03/2022
Combined File of all Documents
Ta dokument ne obstaja v tem jeziku (slovenščina). Spodaj ga najdete v drugem jeziku.
Greek (PDF)
Objavljeno na: 17/06/2024
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