Seliverm, 15mg, Spot-on solution

Ima dovoljenje za promet

Selamectin

Prenes kot PDF

Informacije o zdravilu

Ime zdravila:

Seliverm, 15mg, Spot-on solution

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

Pot uporabe:

Nanos na kožo

Podatki o zdravilu

Učinkovina / Jakost:

Na voljo samo v English

15.00

milligram(s)

/

1.00

Pipeta

Farmacevtska oblika:

Kožni nanos, raztopina

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

QP54AA05

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 Lithuanian Dutch Portuguese Romanian Slovak Swedish Icelandic Norwegian

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 French Italian Latvian Lithuanian Norwegian

Imetnik dovoljenja za promet z zdravilom:

Bioveta a.s.

Datum dovoljenja za promet z zdravilom:

7/10/2024

Proizvodna mesta, odgovorna za sproščanje serij:

Bioveta a.s.

Pristojni organ:

Institute For Control Of Biological Products And Veterinary Medicines

Številka dovoljenja za promet z zdravilom:

240127

Datum spremembe statusa dovoljenja za promet:

7/10/2024

Referenčna država članica:

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

Številka postopka:

CZ/V/0186/001

Zadevne države članice:

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

Generic of:

600000003546

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). Lahko ga najdete spodaj v drugem jeziku.

Drugi jeziki (1)

Romanian (PDF)

Objavljeno na dan: 22/10/2024

Prenesi