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

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Identifikacija zdravila

Ime zdravila:

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

SALMOPORC LYOPHILISAT ET SOLVANT POUR SUSPENSION INJECTABLE / LYOPHILISAT POUR ADMINISTRATION DANS L’EAU DE BOISSON

Učinkovina:

Na voljo samo v English

Ciljne živalske vrste:

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

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Na voljo samo v English

Dodatne informacije

Entitlement type:

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Pravna podlaga za izdajo dovoljenja za promet z zdravilom:

Na voljo samo v English Italian

Imetnik dovoljenja za promet z zdravilom:

Ceva Sante Animale

Marketing authorisation date:

16/08/2023

Proizvodna mesta, odgovorna za sproščanje serij:

Ceva-Phylaxia Zrt.
IDT Biologika GmbH

Pristojni organ:

French Agency For Food, Environmental And Occupational Health & Safety

Številka dovoljenja :

FR/V/7172249 4/2023

Datum spremembe statusa dovoljenja:

16/08/2023

Referenčna država članica:

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

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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