Dectomax Solution Injectable 10 mg/ml Solution injectable

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Doramectin

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Identifikacija proizvoda

Naziv VMP-a:

Dectomax Solution Injectable 10 mg/ml Solution injectable

Dectomax Injektionlösung 10 mg/ml Injektionslösung

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

Način primjene:

Intramuskularno
Supkutano

Pojedinosti o proizvodu

Djelatna tvar i jačina:

Dostupno samo u English

10.00

miligram

/

1.00

mililitar

Farmaceutski oblik:

otopina za injekciju

Withdrawal period by route of administration:

Intramuskularno
- Sheep
  - Meat and offal
    
    70
    
    day
  - Milk
    
    no withdrawal period
Supkutano
- Cattle
  - Meat and offal
    
    70
    
    day
  - Milk
    
    no withdrawal period
    
    Not permitted for use in lactating animals producing milk for human consumption. Do not use in pregnant cows or heifers, which are intended to produce milk for human consumption, within 2 months of expected parturition

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

QP54AA03

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:

Luxembourg

Opis paketa:

Dostupno samo u English
Dostupno samo u English
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 GmbH

Marketing authorisation date:

30/10/1995

Mjesta proizvodnje za izdavanje serije:

Elanco France S.A.S
Norbrook Laboratories Limited

Odgovorno tijelo:

Ministere De La Sante Division De La Pharmacie Et Des Medicaments

Broj autorizacije:

V 867/96/01/0495

Datum promjene statusa odobrenja:

30/10/1995

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

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