SYMPAGESIC 500 MG/ML + 4 MG/ML SOLUTION FOR INJECTION FOR HORSES, CATTLE, PIGS AND DOGS
SYMPAGESIC 500 MG/ML + 4 MG/ML SOLUTION FOR INJECTION FOR HORSES, CATTLE, PIGS AND DOGS
Ima dovoljenje za promet
- Metamizole sodium monohydrate
- Hyoscine butylbromide
Informacije o zdravilu
Ime zdravila:
SYMPAGESIC 500 MG/ML + 4 MG/ML SOLUTION FOR INJECTION FOR HORSES, CATTLE, PIGS AND DOGS
SYMPAGESIC (500+4)MG/ML ΕΝΕΣΙΜΟ ΔΙΑΛΥΜΑ
Ciljne živalske vrste:
-
govedo
Pot uporabe:
-
intramuskularna uporaba
-
Intravenska uporaba
Podatki o zdravilu
Farmacevtska oblika:
-
Raztopina za injiciranje
Karenca glede na pot uporabe:
-
intramuskularna uporaba
-
govedo
-
Meat and offal28day
-
Milkno withdrawal periodNot 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 offal15day
-
-
-
Intravenska uporaba
-
govedo
-
Meat and offal18day
-
Milkno withdrawal periodNot 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 offal15day
-
-
Horse
-
Meat and offal15day
-
-
Horse (mare)
-
Milkno withdrawal periodNot 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):
- QA03DB04
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:
- Dechra Regulatory B.V.
Datum dovoljenja za promet z zdravilom:
Proizvodna mesta, odgovorna za sproščanje serij:
- Genera d.d.
Pristojni organ:
- National Organization For Medicines
Številka dovoljenja za promet z zdravilom:
- 19584/21-02-2025/K-0236101
Datum spremembe statusa dovoljenja za promet:
Številka postopka:
- FR/V/0354/001
Zadevne države članice:
Za poročila o domnevnih neželenih učinkih zdravil za uporabo v veterinaski medicini obiščite stran: www.adrreports.eu/vet
Dokumenti
Povzetek glavnih značilnosti zdravila
Ta dokument ne obstaja v tem jeziku (slovenščina). Spodaj ga najdete v drugem jeziku.
Greek (PDF)
Objavljeno na dan: 5/03/2025
Navodilo za uporabo
Ta dokument ne obstaja v tem jeziku (slovenščina). Spodaj ga najdete v drugem jeziku.
Greek (PDF)
Objavljeno na dan: 5/03/2025
