Veterinary Medicines

Lachesis D8, Flüssige Verdünnung zur Injektion

Pooblaščeno

LACHESIS MUTUS DIL. D8

Download as PDF

Identifikacija zdravila

Ime zdravila:

Lachesis D8, Flüssige Verdünnung zur Injektion

Učinkovina:

Na voljo samo v English

Ciljne živalske vrste:

govedo
tele
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 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

Pot uporabe:

Subkutana uporaba

Podatki o zdravilu

Učinkovina / Jakost:

Na voljo samo v English

100.00

millilitre(s)

/

100.00

millilitre(s)

Farmacevtska oblika:

Raztopina za injiciranje

Pravni status za dobavo / izdajo zdravila:

Zdravilo, ki se izdaja brez veterinarskega recepta

Status dovoljenja:

Valid

Authorised in:

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

Opis ovojnine:

Na voljo samo v German
Na voljo samo v German
Na voljo samo v German
Na voljo samo v German

Dodatne informacije

Entitlement type:

Na voljo samo v English French Italian Latvian Swedish Icelandic Norwegian

Imetnik dovoljenja za promet z zdravilom:

ZIEGLER GmbH Homoeopathika ad us. vet.

Marketing authorisation date:

12/02/1998

Pristojni organ:

Federal Office Of Consumer Protection And Food Safety

Številka dovoljenja :

31951.00.00

Datum spremembe statusa dovoljenja:

16/02/2011

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

Kako koristna je bila ta stran?: