DEPEDIN VEYX, injekcinė suspensija arkliams, galvijams, šunims ir katėms

Ovlašten

Prednisolone acetate
Dexamethasone

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Identifikacija proizvoda

Naziv VMP-a:

DEPEDIN VEYX, injekcinė suspensija arkliams, galvijams, šunims ir katėms

Djelatna tvar:

Dostupno samo u English
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 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
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

Način primjene:

Intramuskularno
Intraartikularno

Pojedinosti o proizvodu

Djelatna tvar i jačina:

Dostupno samo u English

7.50

miligram

/

1.00

mililitar
Dostupno samo u English

2.50

miligram

/

1.00

mililitar

Farmaceutski oblik:

suspenzija za injekciju

Withdrawal period by route of administration:

Intramuskularno
- Horse
  - Meat and offal, milk
    
    no withdrawal period
    
    Not authorized for use in horses, whose meat or milk are meant for human consumption.
- Cattle
  - Meat
    
    10
    
    day
  - Milk
    
    2
    
    day
- Dog
- Cat
Intraartikularno
- Horse
  - Meat and offal, milk
    
    no withdrawal period
    
    Not authorized for use in horses, whose meat or milk are meant for human consumption.
- Cattle
  - Meat
    
    10
    
    day
  - Milk
    
    2
    
    day
- Dog
- Cat

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

QH02AB30

Pravni status opskrbe:

Te informacije nisu dostupne za ovaj lijek.

Status odobrenja:

Važeće

Authorised in:

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

Available in:

Lithuania

Opis paketa:

Dostupno samo u Lithuanian

Dodatne informacije

Entitlement type:

Marketing Authorisation

Pravna osnova za odobrenje proizvoda:

Dostupno samo u English French Italian Latvian Lithuanian Norwegian

Nositelj odobrenja za stavljanje u promet:

Veyx Pharma GmbH

Marketing authorisation date:

29/03/1993

Mjesta proizvodnje za izdavanje serije:

Veyx Pharma GmbH

Odgovorno tijelo:

State Food And Veterinary Service

Broj autorizacije:

LT/2/93/0032/001

Datum promjene statusa odobrenja:

29/07/2006

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

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