NARKAMON 50 mg/ml injekčný roztok

Ima dovoljenje za promet

Ketamine hydrochloride

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Informacije o zdravilu

Ime zdravila:

NARKAMON 50 mg/ml injekčný roztok

Učinkovina:

Na voljo samo v English

Ciljne živalske vrste:

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

Pot uporabe:

intramuskularna uporaba
Intraperitonealna uporaba
Intravenska uporaba

Podatki o zdravilu

Učinkovina / Jakost:

Na voljo samo v English

57.70

milligram(s)

/

1.00

millilitre(s)

Farmacevtska oblika:

Raztopina za injiciranje

Karenca glede na pot uporabe:

intramuskularna uporaba
- tele
  - Meat and offal
    
    24
    
    hour
- Sheep
  - Meat and offal
    
    24
    
    hour
  - Milk
    
    0
    
    day
    
    milk zero days
- Goat
  - Meat and offal
    
    24
    
    hour
  - Milk
    
    0
    
    day
    
    milk zero days
- Dog
  - Not applicable
    
    0
    
    day
    
    Not applicable
- Cat
  - Not applicable
    
    0
    
    day
    
    Not applicable
- Guinea pig
  - Not applicable
    
    0
    
    day
    
    Not applicable
- Monkey
  - Not applicable
    
    0
    
    day
    
    Not applicable
- Parrot
  - Not applicable
    
    0
    
    day
    
    Not applicable
- plazilec
  - Not applicable
    
    0
    
    day
    
    Not applicable
- Antelope
  - Meat and offal
    
    24
    
    hour
- Roe deer
  - Meat and offal
    
    24
    
    hour
- Pigeon
  - Meat and offal
    
    24
    
    hour
- Red deer
  - Meat and offal
    
    24
    
    hour
Intraperitonealna uporaba
- Mouse
  - Not applicable
    
    0
    
    day
    
    Not applicable
- Rat
  - Not applicable
    
    0
    
    day
    
    Not applicable
Intravenska uporaba
- Horse
  - Meat and offal
    
    24
    
    hour
  - Milk
    
    0
    
    day
    
    milkmzreo days
- Dog
  - Not applicable
    
    0
    
    day
    
    Not applicable

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

QN01AX03

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 Slovak

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:

Bioveta a.s.

Datum dovoljenja za promet z zdravilom:

26/09/1988

Proizvodna mesta, odgovorna za sproščanje serij:

Bioveta a.s.

Pristojni organ:

Institute For State Control Of Veterinary Biologicals And Medicaments

Številka dovoljenja za promet z zdravilom:

99/172/88-C/S

Datum spremembe statusa dovoljenja za promet:

26/09/1988

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

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