Receptal 0.004 mg/ml Solution for injection

Ima dovoljenje za promet

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Informacije o zdravilu

Ime zdravila:

Receptal 0.004 mg/ml Solution for injection

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 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 Estonian English French Italian Latvian Lithuanian Hungarian Dutch Romanian Finnish Swedish Norwegian

Pot uporabe:

intramuskularna uporaba
Intravenska uporaba
Subkutana uporaba

Podatki o zdravilu

Učinkovina / Jakost:

Na voljo samo v English

0.00

milligram(s)

/

1.00

millilitre(s)

Farmacevtska oblika:

Raztopina za injiciranje

Karenca glede na pot uporabe:

intramuskularna uporaba
- govedo
  - Meat and offal
    
    0
    
    day
  - Milk
    
    0
    
    day
- Horse
  - Meat and offal
    
    0
    
    day
- Rabbit
  - Meat and offal
    
    0
    
    day
- Trout
  - Meat and offal
    
    0
    
    day
Intravenska uporaba
- govedo
  - Meat and offal
    
    0
    
    day
  - Milk
    
    0
    
    day
- Horse
  - Meat and offal
    
    0
    
    day
- Rabbit
  - Meat and offal
    
    0
    
    day
Subkutana uporaba
- govedo
  - Meat and offal
    
    0
    
    day
  - Milk
    
    0
    
    day
- Horse
  - Meat and offal
    
    0
    
    day
- Rabbit
  - Meat and offal
    
    0
    
    day

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

QH01CA90

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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Opis ovojnine zdravila:

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

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

Imetnik dovoljenja za promet z zdravilom:

Intervet International B.V.

Datum dovoljenja za promet z zdravilom:

6/04/2010

Proizvodna mesta, odgovorna za sproščanje serij:

Intervet International GmbH

Pristojni organ:

Institute For Control Of Biological Products And Veterinary Medicines

Številka dovoljenja za promet z zdravilom:

160179

Datum spremembe statusa dovoljenja za promet:

17/03/2026

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

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