GESTAVET OXI, 10 IU/ml Synthetic Oxytocin, ενέσιμο διάλυμα

Ima dovoljenje za promet

Oxytocin

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Informacije o zdravilu

Ime zdravila:

GESTAVET OXI, 10 IU/ml Synthetic Oxytocin, ενέσιμο διάλυμα

Učinkovina:

Na voljo samo v English

Ciljne živalske vrste:

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 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 Czech Danish German Estonian Greek English French Italian Latvian Lithuanian Hungarian Dutch Romanian Finnish Swedish Icelandic Norwegian

Pot uporabe:

intramuskularna uporaba
Intravenska uporaba

Podatki o zdravilu

Učinkovina / Jakost:

Na voljo samo v English

10.00

international unit(s)

/

1.00

millilitre(s)

Farmacevtska oblika:

Raztopina za injiciranje

Karenca glede na pot uporabe:

intramuskularna uporaba
- govedo
  - Meat and offal
    
    12
    
    hour
  - Milk
    
    12
    
    hour
- Sheep (ewe)
  - Milk
    
    12
    
    hour
  - Meat and offal
    
    12
    
    hour
- Pig (female)
  - Meat and offal
    
    12
    
    hour
Intravenska uporaba
- govedo
  - Meat and offal
    
    12
    
    hour
  - Milk
    
    12
    
    hour
- Sheep
  - Meat and offal
    
    12
    
    hour
  - Milk
    
    12
    
    hour
- Pig (female)
  - Meat and offal
    
    12
    
    hour

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

QH01BB02

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 Greek English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian

Opis ovojnine zdravila:

Na voljo samo v Greek

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 Lithuanian Norwegian

Imetnik dovoljenja za promet z zdravilom:

Biogenesis Global S.L.

Datum dovoljenja za promet z zdravilom:

30/04/2004

Proizvodna mesta, odgovorna za sproščanje serij:

Laboratorios Hipra S.A.

Pristojni organ:

Veterinary Services, Ministry Of Agriculture, Natural Resources And Environment

Številka dovoljenja za promet z zdravilom:

CY00062V

Datum spremembe statusa dovoljenja za promet:

17/05/2011

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

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