Nobivac Rabies suspensija injekcijām liellopiem, zirgiem, aitām, kazām, lapsām, mājas seskiem, suņiem un kaķiem

Ima dovoljenje za promet

Rabies virus, strain Pasteur RIV, Inactivated

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Informacije o zdravilu

Ime zdravila:

Nobivac Rabies suspensija injekcijām liellopiem, zirgiem, aitām, kazām, lapsām, mājas seskiem, suņiem un kaķiem

Učinkovina:

Na voljo samo v English

Ciljne živalske vrste:

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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 German Estonian Greek English French Italian Latvian Lithuanian Hungarian Dutch Romanian Finnish Swedish Icelandic Norwegian
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govedo
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Pot uporabe:

intramuskularna uporaba
Subkutana uporaba

Podatki o zdravilu

Učinkovina / Jakost:

Na voljo samo v English

2.00

international unit(s)

/

1.00

unit(s)

Farmacevtska oblika:

Suspenzija za injiciranje

Karenca glede na pot uporabe:

intramuskularna uporaba
- Horse
  - Not specified
    
    0
    
    day
- Goat
  - Not specified
    
    0
    
    day
- govedo
  - Not specified
    
    0
    
    day
- Sheep
  - Not specified
    
    0
    
    day
Subkutana uporaba
- govedo
  - Not specified
    
    0
    
    day
- Sheep
  - Not specified
    
    0
    
    day
- Goat
  - Not specified
    
    0
    
    day
- Horse
  - Not specified
    
    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:

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Na voljo v:

Latvia

Opis ovojnine zdravila:

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Na voljo samo v Latvian

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 Lithuanian Norwegian

Imetnik dovoljenja za promet z zdravilom:

Intervet International B.V.

Datum dovoljenja za promet z zdravilom:

14/10/1993

Proizvodna mesta, odgovorna za sproščanje serij:

Intervet International B.V.

Pristojni organ:

Food And Veterinary Service

Številka dovoljenja za promet z zdravilom:

V/NRP/93/0040

Datum spremembe statusa dovoljenja za promet:

14/10/1993

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

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