Salmoporc, lyophilisate and solvent for suspension for injection / lyophilisate for use in drinking water

Pooblaščeno

Salmonella enterica, subsp. enterica, serovar Typhimurium, histidine-adenine auxotrophic, Live

Identifikacija zdravila

Ime zdravila:

Salmoporc, Lyophilisat und Lösungsmittel zur Herstellung einer Suspension zur Injektion / Lyophilisat zur Anwendung mit Trinkwasser

Učinkovina:

Na voljo samo v English

Ciljne živalske vrste:

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Na voljo samo v Bulgarian Spanish Danish German Estonian English French Italian Latvian Lithuanian Hungarian Dutch Romanian Finnish Swedish Icelandic Norwegian
Na voljo samo v Bulgarian Spanish Czech Danish German Estonian English French Italian Latvian Lithuanian Hungarian Dutch Romanian Finnish Swedish Icelandic Norwegian

Pot uporabe:

Subkutana uporaba
Peroralna uporaba

Podatki o zdravilu

Učinkovina / Jakost:

Na voljo samo v English

5000.00

million colony forming units

/

1.00

Dose

Farmacevtska oblika:

Liofilizat in vehikel za suspenzijo za injiciranje

Withdrawal period by route of administration:

Subkutana uporaba
- Pig
  - Meat and offal
    
    6
    
    week
- Pig (sow for reproduction)
  - Meat and offal
    
    6
    
    week
Peroralna uporaba
- Pig (suckling piglet)
  - Meat and offal
    
    6
    
    week

Anatomsko-terapevtsko-kemična veterinarska oznaka (ATCvet):

QI09AE02

Pravni status za dobavo / izdajo zdravila:

Zdravilo, ki se izdaja na veterinarski recept

Status dovoljenja:

Valid

Authorised in:

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Opis ovojnine:

Na voljo samo v English
Na voljo samo v English

Dodatne informacije

Entitlement type:

Na voljo samo v English French Croatian Italian Latvian Finnish Swedish Icelandic Norwegian

Pravna podlaga za izdajo dovoljenja za promet z zdravilom:

Na voljo samo v English Italian

Imetnik dovoljenja za promet z zdravilom:

Ceva Tiergesundheit GmbH

Marketing authorisation date:

25/07/2002

Proizvodna mesta, odgovorna za sproščanje serij:

Ceva-Phylaxia Veterinary Biologicals Co. Ltd.
IDT Biologika GmbH

Pristojni organ:

Paul-Ehrlich-Institut

Številka dovoljenja :

PEI.V.02340.01.1

Datum spremembe statusa dovoljenja:

14/06/2007

Referenčna država članica:

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Številka postopka:

DE/V/0290/001

Zadevne države članice:

Na voljo samo v Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Na voljo samo v Spanish Czech German Estonian English French Croatian Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian

Za poročila o domnevnih neželenih učinkih zdravil za uporabo v veterinaski medicini obiščite stran: www.adrreports.eu/vet

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