Euthoxin 500 mg/ml solution for injection

Ni pooblaščeno

Pentobarbital sodium

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Identifikacija zdravila

Ime zdravila:

Euthoxin 500 mg/ml solution for injection

Pentoxin 500 mg/ml injektionsvæske, opløsning

Učinkovina:

Na voljo samo v English

Ciljne živalske vrste:

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 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 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 Romanian Finnish Swedish Norwegian
okrasna ptica
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 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
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
govedo
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:

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Podatki o zdravilu

Učinkovina / Jakost:

Na voljo samo v English

500.00

milligram(s)

/

1.00

millilitre(s)

Farmacevtska oblika:

Raztopina za injiciranje

Withdrawal period by route of administration:

Solution for injection
- Dog
- Cat
- Mink
- Ferret
- Hare
- Rabbit
- Guinea pig
- Hamster
- Rat
- Chicken
- Homing pigeon
- okrasna ptica
- Snake
- Turtle
- Lizard
- Frog
- Horse
- govedo
- Pig

Anatomsko-terapevtsko-kemična veterinarska oznaka (ATCvet):

QN51AA01

Pravni status za dobavo / izdajo zdravila:

Zdravilo, ki se izdaja na veterinarski recept

Status dovoljenja:

Surrendered

Authorised in:

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Opis ovojnine:

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Dodatne informacije

Entitlement type:

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Pravna podlaga za izdajo dovoljenja za promet z zdravilom:

Na voljo samo v English Italian Latvian Norwegian

Imetnik dovoljenja za promet z zdravilom:

Chanelle Pharmaceuticals Manufacturing Limited

Marketing authorisation date:

1/07/2016

Proizvodna mesta, odgovorna za sproščanje serij:

Chanelle Pharmaceuticals Manufacturing Limited

Pristojni organ:

Danish Medicines Agency

Številka dovoljenja :

55454

Datum spremembe statusa dovoljenja:

24/01/2024

Referenčna država članica:

Na voljo samo v Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian

Številka postopka:

PT/V/0142/001

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

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Objavljeno na: 29/06/2023

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Euthoxin 500 mg/ml solution for injection

Identifikacija zdravila

Podatki o zdravilu

Dodatne informacije

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