Enrotron 25 mg/ml Solution for injection for dogs, cats, rodents, reptiles and ornamental birds

Ni odobreno

Enrofloxacin

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Informacije o zdravilu

Ime zdravila:

Enrotron 25 mg/ml Solution for injection for dogs, cats, rodents, reptiles and ornamental birds

Učinkovina:

Na voljo samo v English

Ciljne živalske vrste:

plazilec
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 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
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

Pot uporabe:

intramuskularna uporaba
Subkutana uporaba

Podatki o zdravilu

Učinkovina / Jakost:

Na voljo samo v English

25.00

milligram(s)

/

1.00

millilitre(s)

Farmacevtska oblika:

Raztopina za injiciranje

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

QJ01MA90

Pravni status za dobavo/izdajo zdravila:

Zdravilo, ki se izdaja na veterinarski recept

Status dovoljenja za promet z zdravilom:

Revoked

Ima dovoljenje za promet v:

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Opis ovojnine zdravila:

Na voljo samo v English
Na voljo samo v English

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 Latvian Norwegian

Imetnik dovoljenja za promet z zdravilom:

aniMedica GmbH

Datum dovoljenja za promet z zdravilom:

20/02/2012

Proizvodna mesta, odgovorna za sproščanje serij:

aniMedica GmbH
Industrial Veterinaria S.A.

Pristojni organ:

Directorate General For Food And Veterinary

Številka dovoljenja za promet z zdravilom:

431/01/12DFVPT

Datum spremembe statusa dovoljenja za promet:

30/03/2021

Referenčna država članica:

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Številka postopka:

IE/V/0270/001

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

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