Veterinary Medicines

DENAGARD 100 mg/g PREMEZCLA MEDICAMENTOSA

Ima dovoljenje za promet

Tiamulin hydrogen fumarate

Informacije o zdravilu

Ime zdravila:

DENAGARD 100 mg/g PREMEZCLA MEDICAMENTOSA

Učinkovina:

Na voljo samo v English

Ciljne živalske vrste:

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

Pot uporabe:

Dajanje v krmno mešanico

Podatki o zdravilu

Učinkovina / Jakost:

Na voljo samo v English

100.00

milligram(s)

/

1.00

gram(s)

Farmacevtska oblika:

Predmešanica za zdravilno krmno mešanico

Karenca glede na pot uporabe:

Dajanje v krmno mešanico
- Pig
  - Meat and offal
    
    6
    
    day
- Rabbit
  - Meat and offal
    
    0
    
    day
- Chicken (chick, for replacement)
  - Meat and offal
    
    1
    
    day
  - Eggs
    
    0
    
    day
- Chicken (for reproduction)
  - Meat and offal
    
    1
    
    day
  - Eggs
    
    0
    
    day
- brojler
  - Meat and offal
    
    1
    
    day
  - Eggs
    
    0
    
    day
- Turkey (for reproduction)
  - Meat and offal
    
    4
    
    day
- Turkey (for meat production)
  - Meat and offal
    
    4
    
    day
- Chicken (layer hen)
  - Meat and offal
    
    1
    
    day
  - Eggs
    
    0
    
    day

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

QJ01XQ01

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 Croatian Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian

Opis ovojnine zdravila:

Na voljo samo v Spanish

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:

Elanco Spain S.L.

Datum dovoljenja za promet z zdravilom:

2/03/1987

Proizvodna mesta, odgovorna za sproščanje serij:

Andres Pintaluba S.A.

Pristojni organ:

Spanish Agency Of Medicines And Medical Devices

Številka dovoljenja za promet z zdravilom:

2478 ESP

Datum spremembe statusa dovoljenja za promet:

25/12/2021

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

Dokumenti

Označevanje

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Spanish (PDF)

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Povzetek glavnih značilnosti zdravila

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Navodilo za uporabo

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Drugi jeziki (1)

Spanish (PDF)

Objavljeno na dan: 29/11/2023