Latroxin 100 mg/ml solution for injection for cattle, pigs and sheeps
Latroxin 100 mg/ml solution for injection for cattle, pigs and sheeps
Ima dovoljenje za promet
- Tulathromycin
Informacije o zdravilu
Ime zdravila:
Latroxin 100 mg/ml solution for injection for cattle, pigs and sheeps
Latroxin 100 mg/ml Roztwór do wstrzykiwań
Učinkovina:
- Na voljo samo v English
Ciljne živalske vrste:
-
govedo
Pot uporabe:
-
Subkutana uporaba
-
intramuskularna uporaba
Podatki o zdravilu
Učinkovina / Jakost:
-
Na voljo samo v English100.00/milligram(s)1.00millilitre(s)
Farmacevtska oblika:
-
Raztopina za injiciranje
Karenca glede na pot uporabe:
-
Subkutana uporaba
-
govedo
-
Meat and offal22day
-
Milkno withdrawal periodMilk: Not authorised for use in animals producing milk for human consumption. Do not use in pregnant animals, which are intended to produce milk for human consumption, within 2 months of expected parturition
-
-
govedo
-
Meat and offal22day
-
Milkno withdrawal periodMilk: Not authorised for use in animals producing milk for human consumption. Do not use in pregnant animals, which are intended to produce milk for human consumption, within 2 months of expected parturition
-
-
-
intramuskularna uporaba
-
Sheep
-
Meat and offal16day
-
Milkno withdrawal periodMilk: Not authorised for use in animals producing milk for human consumption. Do not use in pregnant animals, which are intended to produce milk for human consumption, within 2 months of expected parturition
-
-
Pig
-
Meat and offal13day
-
-
Sheep
-
Meat and offal16day
-
Milkno withdrawal periodMilk: Not authorised for use in animals producing milk for human consumption. Do not use in pregnant animals, which are intended to produce milk for human consumption, within 2 months of expected parturition
-
-
Anatomsko-terapevtsko-kemična veterinarska oznaka klasifikacija zdravil, ki se uporabljajo v veterini (ATCvet):
- QJ01FA94
Pravni status za dobavo/izdajo zdravila:
-
Zdravilo, ki se izdaja na veterinarski recept
Status dovoljenja za promet z zdravilom:
-
Valid
Dodatne informacije
Imetnik dovoljenja za promet z zdravilom:
- Mevet S.A.
Datum dovoljenja za promet z zdravilom:
Proizvodna mesta, odgovorna za sproščanje serij:
- Mevet S.A.
Pristojni organ:
- Office For Registration Of Medicinal Products Medical Devices And Biocidal Products
Številka dovoljenja za promet z zdravilom:
- 3104
Datum spremembe statusa dovoljenja za promet:
Številka postopka:
- ES/V/0393/001
Zadevne države članice:
Za poročila o domnevnih neželenih učinkih zdravil za uporabo v veterinaski medicini obiščite stran: www.adrreports.eu/vet
Dokumenti
Combined File of all Documents
Ta dokument ne obstaja v tem jeziku (slovenščina). Spodaj ga najdete v drugem jeziku.
English (PDF)
Objavljeno na dan: 24/07/2025
Povzetek glavnih značilnosti zdravila
Ta dokument ne obstaja v tem jeziku (slovenščina). Spodaj ga najdete v drugem jeziku.
Polish (PDF)
Objavljeno na dan: 23/10/2025
Navodilo za uporabo
Ta dokument ne obstaja v tem jeziku (slovenščina). Spodaj ga najdete v drugem jeziku.
Polish (PDF)
Objavljeno na dan: 23/10/2025
Označevanje
Ta dokument ne obstaja v tem jeziku (slovenščina). Spodaj ga najdete v drugem jeziku.
Polish (PDF)
Objavljeno na dan: 23/10/2025
Kako koristna je bila ta stran?:
