COGLAMUNE

Ni odobreno

Clostridium perfringens, type A, alpha toxoid
Clostridium perfringens, type D, epsilon toxoid
Clostridium perfringens, type C, beta toxoid

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Informacije o zdravilu

Ime zdravila:

COGLAMUNE

Učinkovina:

Na voljo samo v English
Na voljo samo v English
Na voljo samo v English

Ciljne živalske vrste:

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

Pot uporabe:

Subkutana uporaba

Podatki o zdravilu

Učinkovina / Jakost:

Na voljo samo v English

2.00

international unit(s)

/

2.00

millilitre(s)
Na voljo samo v English

5.00

international unit(s)

/

2.00

millilitre(s)
Na voljo samo v English

10.00

international unit(s)

/

2.00

millilitre(s)

Farmacevtska oblika:

Suspenzija za injiciranje

Karenca glede na pot uporabe:

Subkutana uporaba
- govedo
  - All relevant tissues
    
    0
    
    day
- Rabbit (for reproduction)
  - All relevant tissues
    
    0
    
    day
- Pig (for fattening)
  - All relevant tissues
    
    0
    
    day
- Rabbit
  - All relevant tissues
    
    0
    
    day
- Sheep
  - All relevant tissues
    
    0
    
    day
- Goat
  - All relevant tissues
    
    0
    
    day

Anatomsko-terapevtsko-kemična veterinarska oznaka klasifikacija zdravil, ki se uporabljajo v veterini (ATCvet):

QI02AB01
QI03AB
QI04AB01
QI08AB
QI09AB12

Pravni status za dobavo/izdajo zdravila:

Zdravilo, ki se izdaja na veterinarski recept

Status dovoljenja za promet z zdravilom:

Surrendered

Ima dovoljenje za promet v:

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Opis ovojnine zdravila:

Na voljo samo v French
Na voljo samo v French

Dodatne informacije

Vrsta dovoljenja:

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Pravna podlaga za izdajo dovoljenja za promet z zdravilom:

Na voljo samo v English French Italian Latvian Norwegian

Imetnik dovoljenja za promet z zdravilom:

Ceva Sante Animale

Datum dovoljenja za promet z zdravilom:

27/05/1983

Proizvodna mesta, odgovorna za sproščanje serij:

CZ Vaccines S.A.U.

Pristojni organ:

French Agency For Food, Environmental And Occupational Health & Safety

Številka dovoljenja za promet z zdravilom:

FR/V/3350147 3/1983

Datum spremembe statusa dovoljenja za promet:

15/05/2024

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

Dokumenti

Povzetek glavnih značilnosti zdravila

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French (PDF)

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