Veterinary Medicines

Aivlosin 625 mg/g - Granules (chickens and turkeys)

Ovlašten

Tylvalosin

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Identifikacija proizvoda

Naziv VMP-a:

Aivlosin 625 mg/g - Granules (chickens and turkeys)

Djelatna tvar:

Dostupno samo u English

Ciljne vrste životinja:

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Način primjene:

U vodi za piće

Pojedinosti o proizvodu

Djelatna tvar i jačina:

Dostupno samo u English

625.00

miligram

/

1.00

Vrećica

Farmaceutski oblik:

Granule za uporabu u vodi za piće

Withdrawal period by route of administration:

U vodi za piće
- Turkey
  - Meat and offal
    
    2
    
    day
    
    2 days
  - Eggs
    
    no withdrawal period
    
    999 days - Not authorised for laying birds
- Chicken
  - Meat and offal
    
    2
    
    day
    
    2 days
  - Egg
    
    0
    
    day
    
    Zero days

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

QJ01FA92

Pravni status opskrbe:

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Status odobrenja:

Važeće

Authorised in:

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

Nositelj odobrenja za stavljanje u promet:

ECO Animal Health Europe Limited

Marketing authorisation date:

9/09/2004

Mjesta proizvodnje za izdavanje serije:

Acme Drugs - S.r.l.
Provet S.A.

Odgovorno tijelo:

European Commission

Broj autorizacije:

Te informacije nisu dostupne za ovaj lijek.

Datum promjene statusa odobrenja:

19/07/2017

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

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