Enzaprost 5 mg/ml raztopina za injiciranje za govedo in prašiče

Ima dovoljenje za promet

Dinoprost trometamol

Prenes kot PDF

Informacije o zdravilu

Ime zdravila:

Enzaprost 5 mg/ml raztopina za injiciranje za govedo in prašiče

Učinkovina:

Na voljo samo v English

Ciljne živalske vrste:

govedo
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

Podatki o zdravilu

Učinkovina / Jakost:

Na voljo samo v English

6.70

milligram(s)

/

1.00

millilitre(s)

Farmacevtska oblika:

Raztopina za injiciranje

Karenca glede na pot uporabe:

intramuskularna uporaba
- govedo
  - Meat and offal
    
    2
    
    day
  - Milk
    
    0
    
    day
- Pig
  - Meat and offal
    
    2
    
    day

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

QG02AD01

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:

Slovenia

Opis ovojnine zdravila:

Na voljo samo v English
Na voljo samo v English
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:

Ceva Sante Animale

Datum dovoljenja za promet z zdravilom:

7/08/2012

Proizvodna mesta, odgovorna za sproščanje serij:

CEVA Santé Animale

Pristojni organ:

Agency For Medicinal Products And Medical Devices Of The Republic Of Slovenia

Številka dovoljenja za promet z zdravilom:

MR/V/0403/001

Datum spremembe statusa dovoljenja za promet:

7/08/2012

Referenčna država članica:

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

Številka postopka:

FR/V/0410/001

Zadevne države članice:

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 Croatian 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 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 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 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 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 Croatian 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 Estonian English French Lithuanian Portuguese Swedish Icelandic Norwegian

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

Dokumenti

Povzetek glavnih značilnosti zdravila

slovenščina (PDF)

Objavljeno na dan: 24/12/2025

Prenesi

Navodilo za uporabo

slovenščina (PDF)

Objavljeno na dan: 24/12/2025

Prenesi

Označevanje

slovenščina (PDF)

Objavljeno na dan: 24/12/2025

Prenesi

Combined File of all Documents

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

Drugi jeziki (1)

English (PDF)

Objavljeno na dan: 14/03/2026

Prenesi