Veterinary Medicines

RAFOXANIDE/PROVET 300MG/TAB ΔΙΣΚΙΟ

Ovlašten

Rafoxanide

Download as PDF

Identifikacija proizvoda

Naziv VMP-a:

RAFOXANIDE/PROVET 300MG/TAB ΔΙΣΚΙΟ

Djelatna tvar:

Dostupno samo u English

Ciljne vrste životinja:

Dostupno samo u Bulgarian Spanish Czech Danish German Estonian Greek English French Italian Latvian Lithuanian Hungarian Dutch Romanian Swedish Icelandic Norwegian

Način primjene:

Kroz usta

Pojedinosti o proizvodu

Djelatna tvar i jačina:

Dostupno samo u English

300.00

miligram

/

1.00

Tableta

Farmaceutski oblik:

Tableta

Withdrawal period by route of administration:

Kroz usta
- Sheep
  - Meat and offal
    
    42
    
    day
    
    ΓΑΛΑ: Δεν επιτρέπεται η χρήση σε θηλθκά πρόβατα που παράγουν γάλα για ανθρώπινη κατανάλωση, περιλαμβανομένης της ξηράς περιόδου και να μην χρησιμοποιείται για ένα έτος πριν από τον πρώτο τοκετό

Kod anatomsko-terapijsko-kemijske klasifikacije (ATKvet kȏd):

QP52AG05

Pravni status opskrbe:

Dostupno samo u Czech Estonian English French Italian Latvian Portuguese Slovenian Finnish Swedish Icelandic Norwegian

Status odobrenja:

Važeće

Authorised in:

Dostupno samo u Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian

Opis paketa:

Dostupno samo u Greek

Dodatne informacije

Entitlement type:

Marketing Authorisation

Pravna osnova za odobrenje proizvoda:

Dostupno samo u English

Nositelj odobrenja za stavljanje u promet:

Provet S.A.

Marketing authorisation date:

28/03/1989

Mjesta proizvodnje za izdavanje serije:

Provet S.A.

Odgovorno tijelo:

National Organization For Medicines

Broj autorizacije:

89517/15-12-2009/K-0041601

Datum promjene statusa odobrenja:

11/10/2021

To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet

Koliko je bila korisna ova stranica?: