TELMIN 20mg/ml suspensão oral

Ima dovoljenje za promet

Mebendazole

Prenes kot PDF

Informacije o zdravilu

Ime zdravila:

TELMIN 20mg/ml suspensão oral

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 Estonian Greek English French Italian Latvian Lithuanian Hungarian Dutch Romanian Finnish Swedish 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:

Peroralna uporaba

Podatki o zdravilu

Učinkovina / Jakost:

Na voljo samo v English

20.00

milligram(s)

/

1.00

millilitre(s)

Farmacevtska oblika:

Peroralna suspenzija

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

QP52AC09

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

Na voljo v:

Portugal

Opis ovojnine zdravila:

Na voljo samo v Portuguese

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:

Ecuphar Veterinaria S.L.U.

Datum dovoljenja za promet z zdravilom:

11/11/1999

Proizvodna mesta, odgovorna za sproščanje serij:

Divasa Farmavic S.A.

Pristojni organ:

Directorate General For Food And Veterinary

Številka dovoljenja za promet z zdravilom:

51284

Datum spremembe statusa dovoljenja za promet:

19/04/2022

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

Dokumenti

Combined File of all Documents

Ta dokument ne obstaja v tem jeziku (slovenščina). Spodaj ga najdete v drugem jeziku.

Drugi jeziki (1)

Portuguese (PDF)

Objavljeno na dan: 26/11/2024

Prenesi