KANAMUCIL

Ima dovoljenje za promet

Acetylcysteine
Kanamycin sulfate

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Informacije o zdravilu

Ime zdravila:

KANAMUCIL

Učinkovina:

Na voljo samo v English
Na voljo samo v English

Ciljne živalske vrste:

govedo
brojler
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
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:

Endotraheopulmonalna uporaba
intramuskularna uporaba
Subkutana uporaba
Intrauterina uporaba

Podatki o zdravilu

Učinkovina / Jakost:

Na voljo samo v English

7.50

gram(s)

/

100.00

millilitre(s)
Na voljo samo v English

7500000.00

international unit(s)

/

100.00

millilitre(s)

Farmacevtska oblika:

Raztopina za injiciranje

Karenca glede na pot uporabe:

Endotraheopulmonalna uporaba
- govedo
  - Meat and offal
    
    29
    
    day
  - Milk
    
    6
    
    day
- brojler
  - Meat and offal
    
    22
    
    day
    
    Uso non autorizzato in uccelli che producono uova per il consumo umano
- Goat
  - Meat and offal
    
    29
    
    day
  - Milk
    
    6
    
    day
- Sheep
  - Meat and offal
    
    29
    
    day
  - Milk
    
    6
    
    day
- Pig
  - Meat and offal
    
    29
    
    day
- Horse
  - Meat and offal
    
    29
    
    day
    
    Uso non autorizzato in equidi che producono latte per il consumo umano
intramuskularna uporaba
- govedo
  - Meat and offal
    
    29
    
    day
  - Milk
    
    6
    
    day
- brojler
  - Meat and offal
    
    22
    
    day
    
    Uso non autorizzato in uccelli che producono uova per il consumo umano
- Goat
  - Meat and offal
    
    29
    
    day
  - Meat and offal
    
    29
    
    day
- Sheep
  - Meat and offal
    
    29
    
    day
  - Milk
    
    6
    
    day
- Pig
  - Meat and offal
    
    29
    
    day
- Horse
  - Meat and offal
    
    29
    
    day
    
    Uso non autorizzato in equidi che producono latte per il consumo umano
Subkutana uporaba
- brojler
  - Meat and offal
    
    22
    
    day
Intrauterina uporaba
- govedo
  - Meat and offal
    
    29
    
    day
  - Milk
    
    6
    
    day
- brojler
  - Meat and offal
    
    22
    
    day
    
    Uso non autorizzato in uccelli che producono uova per il consumo umano
- Goat
  - Meat and offal
    
    29
    
    day
  - Milk
    
    6
    
    day
- Sheep
  - Meat and offal
    
    29
    
    day
  - Milk
    
    6
    
    day
- Pig
  - Meat and offal
    
    29
    
    day
- Horse
  - Meat and offal
    
    29
    
    day
    
    Uso non autorizzato in equidi che producono latte per il consumo umano

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

QJ01RV01

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 Italian
Na voljo samo v Italian
Na voljo samo v Italian
Na voljo samo v Italian

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 Productions S.r.l.

Datum dovoljenja za promet z zdravilom:

2/01/1987

Proizvodna mesta, odgovorna za sproščanje serij:

Intervet Productions S.r.l.

Pristojni organ:

Ministry Of Health

Številka dovoljenja za promet z zdravilom:

Ta podatek za to zdravilo ni na voljo.

Datum spremembe statusa dovoljenja za promet:

18/09/1997

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

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Objavljeno na dan: 3/06/2022

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