Bravoxin 10 suspension for injection for cattle and sheep
Bravoxin 10 suspension for injection for cattle and sheep
Pooblaščeno
- Clostridium novyi, type D, toxoid
- Clostridium sordellii, toxoid
- Tetanus toxoid adsorbed
- Clostridium septicum, toxoid
- Clostridium novyi, toxoid
- Clostridium chauvoei, Inactivated
- Clostridium perfringens, type D, epsilon toxoid
- Clostridium perfringens, type C, beta toxoid
- Clostridium perfringens, type B, beta toxoid
- Clostridium perfringens, type A, alpha toxoid
Identifikacija zdravila
Ime zdravila:
Bravoxin 10 suspension for injection for cattle and sheep
Bravoxin 10 suspensão injetável para bovinos e ovinos
Pot uporabe:
-
Subkutana uporaba
Podatki o zdravilu
Učinkovina / Jakost:
-
Na voljo samo v English17.40unit(s)1.00millilitre(s)
-
Na voljo samo v English4.40international unit(s)1.00millilitre(s)
-
Na voljo samo v English4.90international unit(s)1.00millilitre(s)
-
Na voljo samo v English4.60international unit(s)1.00millilitre(s)
-
Na voljo samo v English3.80international unit(s)1.00millilitre(s)
-
Na voljo samo v English90.00percentage protection1.00millilitre(s)
-
Na voljo samo v English5.30international unit(s)1.00millilitre(s)
-
Na voljo samo v English18.20international unit(s)1.00millilitre(s)
-
Na voljo samo v English18.20international unit(s)1.00millilitre(s)
-
Na voljo samo v English0.50enzyme-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
-
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:
- European Medicines Agency
Marketing authorisation date:
Proizvodna mesta, odgovorna za sproščanje serij:
- MSD Animal Health UK Limited
- INTERVET INTERNATIONAL B.V.
Pristojni organ:
- European Medicines Agency
Številka dovoljenja :
- 807/08 DIVPT
Datum spremembe statusa dovoljenja:
Številka postopka:
- DE/V/0279/001
Zadevne države članice:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Dokumenti
Povzetek glavnih značilnosti zdravila
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English (PDF)
Objavljeno na: 28/01/2022
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