NEOMYCINE 50 COOPHAVET POUDRE POUR SOLUTION BUVABLE

Ima dovoljenje za promet

NEOMYCIN SULFATE

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Informacije o zdravilu

Ime zdravila:

NEOMYCINE 50 COOPHAVET POUDRE POUR SOLUTION BUVABLE

Učinkovina:

Na voljo samo v English

Ciljne živalske vrste:

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

Peroralna uporaba

Podatki o zdravilu

Učinkovina / Jakost:

Na voljo samo v English

500000.00

international unit(s)

/

1.00

gram(s)

Farmacevtska oblika:

Prašek za peroralno raztopino

Karenca glede na pot uporabe:

Peroralna uporaba
- govedo
  - Milk
    
    no withdrawal period
    
    Ne pas utiliser chez les animaux producteurs de lait destiné à la consommation humaine
- Pig (piglet)
  - Meat and offal
    
    14
    
    day
- Rabbit
  - Meat and offal
    
    14
    
    day
- Sheep (lamb)
  - Meat and offal
    
    14
    
    day
- Sheep
  - Milk
    
    no withdrawal period
    
    Ne pas utiliser chez les animaux producteurs de lait destiné à la consommation humaine
- Goat (kid)
  - Meat and offal
    
    14
    
    day
- Goat
  - Milk
    
    no withdrawal period
    
    Ne pas utiliser chez les animaux producteurs de lait destiné à la consommation humaine
- tele
  - Meat and offal
    
    14
    
    day
- Poultry
  - Meat and offal
    
    14
    
    day
  - Eggs
    
    0
    
    day

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

QA07AA01

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

Opis ovojnine zdravila:

Na voljo samo v French
Na voljo samo v French
Na voljo samo v French
Na voljo samo v French
Na voljo samo v French
Na voljo samo v French
Na voljo samo v French
Na voljo samo v French

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 French Italian Latvian Norwegian

Imetnik dovoljenja za promet z zdravilom:

Dopharma France S.A.S.

Datum dovoljenja za promet z zdravilom:

18/06/1992

Proizvodna mesta, odgovorna za sproščanje serij:

Dopharma France

Pristojni organ:

French Agency For Food, Environmental And Occupational Health & Safety

Številka dovoljenja za promet z zdravilom:

FR/V/0359766 8/1992

Datum spremembe statusa dovoljenja za promet:

18/06/2012

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

Dokumenti

Povzetek glavnih značilnosti zdravila

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Package Leaflet and Labelling

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Drugi jeziki (1)

French (PDF)

Objavljeno na dan: 15/10/2025

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