Apralan Soluble Powder for Use in Drinking Water/Milk Replacer for Pigs, Calves, Chickens and Rabbits

Pooblaščeno

Apramycin sulfate

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Identifikacija zdravila

Ime zdravila:

GIROLAN/APRALAN

Apralan Soluble Powder for Use in Drinking Water/Milk Replacer for Pigs, Calves, Chickens and Rabbits

Učinkovina:

Na voljo samo v English

Ciljne živalske vrste:

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Na voljo samo v Bulgarian Spanish Czech Danish Estonian Greek English French Italian Latvian Lithuanian Hungarian Dutch Romanian Swedish Icelandic Norwegian
Na voljo samo v Bulgarian Spanish Czech Danish German Estonian English French Italian Latvian Lithuanian Hungarian Dutch Romanian Swedish Norwegian
brojler

Pot uporabe:

Dajanje v vodo za pitje/mleko

Podatki o zdravilu

Učinkovina / Jakost:

Na voljo samo v English

552000.00

international unit(s)

/

1.00

gram(s)

Farmacevtska oblika:

Prašek za dajanje v vodo za pitje/mleko

Withdrawal period by route of administration:

Dajanje v vodo za pitje/mleko
- Pig (weaned piglet)
  - Meat and offal
    
    0
    
    day
- Rabbit
  - Meat and offal
    
    0
    
    day
- Cattle (pre-ruminant)
  - Meat and offal
    
    28
    
    day
- brojler
  - Meat and offal
    
    0
    
    day
  - Eggs
    
    no withdrawal period
    
    Eggs: Not authorised for use in laying birds producing eggs for human consumption. Do not use within 4 weeks of onset of the laying period.

Anatomsko-terapevtsko-kemična veterinarska oznaka (ATCvet):

QJ01GB90

Pravni status za dobavo / izdajo zdravila:

Zdravilo, ki se izdaja na veterinarski recept

Status dovoljenja:

Valid

Authorised in:

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Opis ovojnine:

Na voljo samo v English
Na voljo samo v English
Na voljo samo v English
Na voljo samo v English

Dodatne informacije

Entitlement type:

Na voljo samo v English French Croatian Italian Latvian Finnish Swedish Icelandic Norwegian

Pravna podlaga za izdajo dovoljenja za promet z zdravilom:

Na voljo samo v English Italian Latvian Norwegian

Imetnik dovoljenja za promet z zdravilom:

Eli Lilly And Company Limited

Marketing authorisation date:

20/10/1992

Proizvodna mesta, odgovorna za sproščanje serij:

Elanco France S.A.S

Pristojni organ:

The Veterinary Medicines Directorate

Številka dovoljenja :

Vm 00006/4084

Datum spremembe statusa dovoljenja:

15/08/2022

Referenčna država članica:

Na voljo samo v Spanish Czech German Estonian English French Croatian Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian

Številka postopka:

ES/V/0321/001

Zadevne države članice:

Na voljo samo v Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Na voljo samo v Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Na voljo samo v Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Na voljo samo v Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Na voljo samo v Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Na voljo samo v Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Na voljo samo v Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Na voljo samo v Estonian English French Swedish Icelandic Norwegian

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

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