Isothesia 1000 mg/g inhalation vapour, liquid for horses, dogs, cats, ornamental birds, reptiles, rats, mice, hamsters, chinchillas, gerbils, guinea pigs and ferrets

Ni odobreno

Isoflurane

Informacije o zdravilu

Ime zdravila:

Učinkovina:

Na voljo samo v English

Ciljne živalske vrste:

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okrasna ptica
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 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 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
plazilec

Pot uporabe:

Za inhaliranje

Podatki o zdravilu

Učinkovina / Jakost:

Na voljo samo v English

1000.00

milligram(s)

/

1.00

millilitre(s)

Farmacevtska oblika:

Para za inhaliranje, tekočina

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

QN01AB06

Pravni status za dobavo/izdajo zdravila:

Zdravilo, ki se izdaja na veterinarski recept

Status dovoljenja za promet z zdravilom:

Surrendered

Ima dovoljenje za promet v:

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Opis ovojnine zdravila:

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Na voljo samo v English

Dodatne informacije

Vrsta dovoljenja:

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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:

Zoetis B.V.

Datum dovoljenja za promet z zdravilom:

11/04/2014

Proizvodna mesta, odgovorna za sproščanje serij:

Zoetis Belgium

Pristojni organ:

Medicines Evaluation Board

Številka dovoljenja za promet z zdravilom:

REG NL 113697

Datum spremembe statusa dovoljenja za promet:

3/04/2023

Referenčna država članica:

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Številka postopka:

ES/V/0173/001

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

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Objavljeno na dan: 17/01/2022

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