Revet RV 6

Ima dovoljenje za promet

Acidum arsenicosum C9
Podophyllum peltatum C6
Rheum C6

Prenes kot PDF

Informacije o zdravilu

Ime zdravila:

Revet RV 6

Učinkovina:

Na voljo samo v English
Na voljo samo v English
Na voljo samo v English

Ciljne živalske vrste:

Na voljo samo v Bulgarian Spanish Czech Danish German Estonian English French Italian Latvian Lithuanian Hungarian Dutch Romanian Finnish Swedish Icelandic Norwegian
Na voljo samo v Bulgarian Spanish Danish German Estonian English French Italian Latvian Lithuanian Hungarian Dutch Romanian Finnish Swedish Norwegian
govedo
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 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 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
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 English French Italian Latvian Lithuanian Hungarian Dutch Romanian Finnish Swedish 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 Czech Danish German Estonian Greek English French Italian Latvian Lithuanian Hungarian Dutch Romanian Finnish Swedish Norwegian
Na voljo samo v Bulgarian Spanish Czech Danish Estonian English French Italian Latvian Lithuanian Hungarian Dutch Romanian Finnish Swedish Norwegian
Na voljo samo v Bulgarian Spanish Czech Danish Estonian English French Italian Latvian Lithuanian Hungarian Dutch Romanian Finnish Swedish Norwegian

Pot uporabe:

intramuskularna uporaba
Dajanje v vodo za pitje
Subkutana uporaba
Intravenska uporaba
Kopanje

Podatki o zdravilu

Učinkovina / Jakost:

Na voljo samo v English

0.33

gram(s)

/

1.00

millilitre(s)
Na voljo samo v English

0.33

gram(s)

/

1.00

millilitre(s)
Na voljo samo v English

0.33

gram(s)

/

1.00

millilitre(s)

Farmacevtska oblika:

Raztopina za injiciranje

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

Opis ovojnine zdravila:

Na voljo samo v German

Dodatne informacije

Vrsta dovoljenja:

Na voljo samo v English French Italian Latvian Swedish Icelandic Norwegian

Imetnik dovoljenja za promet z zdravilom:

Pharmazeutische Fabrik Dr. Reckeweg & Co. GmbH

Datum dovoljenja za promet z zdravilom:

6/04/2000

Proizvodna mesta, odgovorna za sproščanje serij:

Pharmazeutische Fabrik Dr. Reckeweg & Co. GmbH

Pristojni organ:

Federal Office Of Consumer Protection And Food Safety

Številka dovoljenja za promet z zdravilom:

31898.00.00

Datum spremembe statusa dovoljenja za promet:

13/07/2012

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