RABISIN, ενέσιμο εναιώρημα

Pooblaščeno

Rabies virus, strain G52, Inactivated

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Identifikacija zdravila

Ime zdravila:

RABISIN, ενέσιμο εναιώρημα

Učinkovina:

Na voljo samo v English

Ciljne živalske vrste:

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

Pot uporabe:

intramuskularna uporaba
Subkutana uporaba

Podatki o zdravilu

Učinkovina / Jakost:

Na voljo samo v English

2.09

log 10 optical density 50

/

1.00

dose

Farmacevtska oblika:

Suspenzija za injiciranje

Withdrawal period by route of administration:

intramuskularna uporaba
- Horse
  - Not applicable
    
    no withdrawal period
- govedo
  - Not applicable
    
    no withdrawal period
- Sheep
  - Not applicable
    
    no withdrawal period
- Dog
  - Not applicable
    
    no withdrawal period
- Cat
  - Not applicable
    
    no withdrawal period
- Ferret
  - Not applicable
    
    no withdrawal period
Subkutana uporaba
- govedo
  - Not applicable
    
    no withdrawal period
- Sheep
  - Not applicable
    
    no withdrawal period
- Dog
  - Not applicable
    
    no withdrawal period
- Cat
  - Not applicable
    
    no withdrawal period
- Ferret
  - Not applicable
    
    no withdrawal period

Anatomsko-terapevtsko-kemična veterinarska oznaka (ATCvet):

QI07AA02

Pravni status za dobavo / izdajo zdravila:

Zdravilo, ki se izdaja na veterinarski recept

Status dovoljenja:

Valid

Authorised in:

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Available in:

Greece

Opis ovojnine:

Na voljo samo v Greek
Na voljo samo v Greek
Na voljo samo v Greek
Na voljo samo v Greek
Na voljo samo v Greek

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

Imetnik dovoljenja za promet z zdravilom:

Boehringer Ingelheim Animal Health France

Marketing authorisation date:

28/01/1987

Proizvodna mesta, odgovorna za sproščanje serij:

Boehringer Ingelheim Animal Health France

Pristojni organ:

National Organization For Medicines

Številka dovoljenja :

57429/02-06-2020/K-0013001

Datum spremembe statusa dovoljenja:

22/06/2021

To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet

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