EXFLOW 10 MG/G POWDER FOR USE IN DRINKING WATER FOR CATTLE (CALVES), PIGS, CHICKENS, TURKEYS AND DUCKS

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Bromhexine hydrochloride

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Informacije o zdravilu

Ime zdravila:

EXFLOW 10 MG/G POWDER FOR USE IN DRINKING WATER FOR CATTLE (CALVES), PIGS, CHICKENS, TURKEYS AND DUCKS

EXFLOW 10 mg/g pulbere pentru administrare în apa de băut pentru bovine (viței), porci, pui de găină, curci și rațe

Učinkovina:

Na voljo samo v English

Ciljne živalske vrste:

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tele
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brojler

Pot uporabe:

Peroralna uporaba

Podatki o zdravilu

Učinkovina / Jakost:

Na voljo samo v English

10.00

milligram(s)

/

1.00

gram(s)

Farmacevtska oblika:

Prašek za dajanje v vodo za pitje

Karenca glede na pot uporabe:

Peroralna uporaba
- Turkey
  - Meat and offal
    
    0
    
    day
  - Eggs
    
    no withdrawal period
    
    Do not use in birds producing eggs for consumption, during and 4 weeks before the laying phase.
- Pig
  - Meat and offal
    
    0
    
    day
- tele
  - Meat and offal
    
    2
    
    day
  - Milk
    
    no withdrawal period
    
    Not permitted for use in cows producing milk for human consumption.
- Duck
  - Meat and offal
    
    0
    
    day
  - Eggs
    
    no withdrawal period
    
    Do not use in birds producing eggs for consumption, during and 4 weeks before the laying phase.
- brojler
  - Meat and offal
    
    0
    
    day
  - Eggs
    
    no withdrawal period
    
    Do not use in birds producing eggs for consumption, during and 4 weeks before the laying phase.

Anatomsko-terapevtsko-kemična veterinarska oznaka klasifikacija zdravil, ki se uporabljajo v veterini (ATCvet):

QR05CB02

Pravni status za dobavo/izdajo zdravila:

Zdravilo, ki se izdaja na veterinarski recept

Status dovoljenja za promet z zdravilom:

Surrendered

Ima dovoljenje za promet v:

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Opis ovojnine zdravila:

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

Dodatne informacije

Vrsta dovoljenja:

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:

Ceva Sante Animale Romania S.R.L.

Datum dovoljenja za promet z zdravilom:

25/08/2015

Proizvodna mesta, odgovorna za sproščanje serij:

Ceva Sante Animale
Laboratoires Biove

Pristojni organ:

Institute For Control Of Biological Products And Veterinary Medicines

Številka dovoljenja za promet z zdravilom:

200079

Datum spremembe statusa dovoljenja za promet:

5/12/2023

Referenčna država članica:

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Številka postopka:

FR/V/0285/001

Za poročila o domnevnih neželenih učinkih zdravil za uporabo v veterinaski medicini obiščite stran: www.adrreports.eu/vet

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