Baytril 25 mg/ml Solution injectable

Ovlašten

Enrofloxacin

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Identifikacija proizvoda

Naziv VMP-a:

Baytril 25 mg/ml Solution injectable

Djelatna tvar:

Dostupno samo u English

Ciljne vrste životinja:

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

Način primjene:

Supkutano

Pojedinosti o proizvodu

Djelatna tvar i jačina:

Dostupno samo u English

25.00

miligram

/

1.00

mililitar

Farmaceutski oblik:

otopina za injekciju

Withdrawal period by route of administration:

Supkutano
- Rabbit
  - Meat and offal
    
    6
    
    day
- Cat
- Pig
  - Meat and offal
    
    13
    
    day
- Dog
- Ornamental bird

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

QJ01MA90

Pravni status opskrbe:

Dostupno samo u Czech Estonian English French Italian Latvian Lithuanian Portuguese Romanian 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:

Luxembourg

Opis paketa:

Dostupno samo u English
Dostupno samo u English

Dodatne informacije

Entitlement type:

Marketing Authorisation

Pravna osnova za odobrenje proizvoda:

Dostupno samo u English Italian

Nositelj odobrenja za stavljanje u promet:

Elanco Animal Health GmbH

Marketing authorisation date:

26/11/1991

Mjesta proizvodnje za izdavanje serije:

KVP Pharma + Veterinaer Produkte GmbH

Odgovorno tijelo:

Ministry Of Health And Social Security

Broj autorizacije:

V/442/91/11/0359

Datum promjene statusa odobrenja:

26/11/1991

Za izvješća o sumnjama na nuspojave veterinarskog lijeka molimo vas otiđite na www.adrreports.eu/vet

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