EXFLOW 10 MG/G POWDER FOR USE IN DRINKING WATER FOR CATTLE (CALVES), PIGS, CHICKENS, TURKEYS AND DUCKS
EXFLOW 10 MG/G POWDER FOR USE IN DRINKING WATER FOR CATTLE (CALVES), PIGS, CHICKENS, TURKEYS AND DUCKS
Ni odobreno
- Bromhexine hydrochloride
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 pó para administração na água de bebida para bovinos (vitelos), suínos, galinhas, perus e patos
Učinkovina:
- Na voljo samo v English
Ciljne živalske vrste:
-
tele
-
brojler
Pot uporabe:
-
Peroralna uporaba
Podatki o zdravilu
Učinkovina / Jakost:
-
Na voljo samo v English10.00/milligram(s)1.00gram(s)
Farmacevtska oblika:
-
Prašek za dajanje v vodo za pitje
Karenca glede na pot uporabe:
-
Peroralna uporaba
-
Turkey
-
Meat and offal0day
-
Eggsno withdrawal periodDo not use in birds producing eggs for consumption, during and 4 weeks before the laying phase.
-
-
Pig
-
Meat and offal0day
-
-
tele
-
Meat and offal2day
-
Milkno withdrawal periodNot permitted for use in cows producing milk for human consumption.
-
-
Duck
-
Meat and offal0day
-
Eggsno withdrawal periodDo not use in birds producing eggs for consumption, during and 4 weeks before the laying phase.
-
-
brojler
-
Meat and offal0day
-
Eggsno withdrawal periodDo 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:
-
Revoked
Dodatne informacije
Imetnik dovoljenja za promet z zdravilom:
- Ceva Saude Animal Produtos Farmaceuticos E Imunologicos Lda.
Datum dovoljenja za promet z zdravilom:
Proizvodna mesta, odgovorna za sproščanje serij:
- Ceva Sante Animale
- LABORATOIRES BIOVE
Pristojni organ:
- Directorate General For Food And Veterinary
Številka dovoljenja za promet z zdravilom:
- 941/01/15RDVPT
Datum spremembe statusa dovoljenja za promet:
Številka postopka:
- FR/V/0285/001
Za poročila o domnevnih neželenih učinkih zdravil za uporabo v veterinaski medicini obiščite stran: www.adrreports.eu/vet