600000040655

Product identification

Naziv VMP-a:

K-VET DOXYCYCLINE 50 MG/G POUDRE

Djelatna tvar:

Te informacije nisu dostupne za ovaj lijek.

Ciljne vrste životinja:

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

Način primjene:

Kroz usta

Product details

Djelatna tvar i jačina:

Te informacije nisu dostupne za ovaj lijek.

Farmaceutski oblik:

Prašak za uporabu u vodi za piće/mlijeku

Withdrawal period by route of administration:

Kroz usta
- Turkey
  - Meat and offal
    
    12
    
    day
    
    En absence de LMR pour les oeufs, ne pas utiliser chez les espèces pondeuses productrices d'oeufs de consommation, 4 semaines avant le démarrage de la ponte et pendant celle-ci.
- Pig
  - Meat and offal
    
    6
    
    day
- Cattle (calf)
  - Meat and offal
    
    14
    
    day
- Chicken (broiler)
  - Meat and offal
    
    7
    
    day
    
    En absence de LMR pour les oeufs, ne pas utiliser chez les espèces pondeuses productrices d'oeufs de consommation, 4 semaines avant le démarrage de la ponte et pendant celle-ci.

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

QJ01AA02

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

Available in:

France

Opis paketa:

Dostupno samo u French
Dostupno samo u French
Dostupno samo u French

Additional information

Entitlement type:

Marketing Authorisation

Pravna osnova za odobrenje proizvoda:

Dostupno samo u English Italian Latvian Norwegian

Nositelj odobrenja za stavljanje u promet:

Huvepharma S.A.

Marketing authorisation date:

7/11/2018

Mjesta proizvodnje za izdavanje serije:

Huvepharma

Odgovorno tijelo:

French Agency For Food, Environmental And Occupational Health & Safety

Broj autorizacije:

FR/V/2548998 1/2018

Datum promjene statusa odobrenja:

7/11/2018

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

Documents

Package Leaflet and Labelling

Ovaj dokument ne postoji na ovom jeziku (hrvatski). U nastavku ga možete pronaći na drugom jeziku.

Ostali jezici (1)

French (PDF)

Objavljeno na: 5/12/2022

Preuzimanje datoteka

Sažetak opisa svojstava lijeka