600000073327

Informacije o zdravilu

Ime zdravila:

Rabisin Injektionssuspension für Hunde, Katzen, Marderartige, Pferde, Rinder und Schafe

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
govedo
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 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 Norwegian

Pot uporabe:

intramuskularna uporaba
Subkutana uporaba

Podatki o zdravilu

Učinkovina / Jakost:

Na voljo samo v English

1.00

international unit(s)

/

1.00

millilitre(s)

Farmacevtska oblika:

Suspenzija za injiciranje

Karenca glede na pot uporabe:

intramuskularna uporaba
- Sheep
  - Meat and offal
    
    0
    
    day
  - Milk
    
    0
    
    day
- govedo
  - Milk
    
    0
    
    day
  - Meat and offal
    
    0
    
    day
- Horse
  - Milk
    
    0
    
    day
  - Meat and offal
    
    0
    
    day
Subkutana uporaba
- govedo
  - Milk
    
    0
    
    day
  - Meat and offal
    
    0
    
    day
- Sheep
  - Meat and offal
    
    0
    
    day
  - Milk
    
    0
    
    day

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

QI07AA02

Pravni status za dobavo/izdajo zdravila:

Zdravilo, ki se izdaja na veterinarski recept

Status dovoljenja za promet z zdravilom:

Valid

Ima dovoljenje za promet v:

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

Na voljo v:

Germany

Opis ovojnine zdravila:

Na voljo samo v German
Na voljo samo v German
Na voljo samo v German

Dodatne informacije

Vrsta dovoljenja:

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 Latvian Norwegian

Imetnik dovoljenja za promet z zdravilom:

Boehringer Ingelheim Vetmedica GmbH

Datum dovoljenja za promet z zdravilom:

24/11/2005

Proizvodna mesta, odgovorna za sproščanje serij:

Boehringer Ingelheim Animal Health France

Pristojni organ:

Paul-Ehrlich-Institut

Številka dovoljenja za promet z zdravilom:

94a/84

Datum spremembe statusa dovoljenja za promet:

20/07/2010

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

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