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 mg/ml + 4 mg/ml Solution for Injection for Horses, Cattle, Pigs and Dogs
Ciljne živalske vrste:
-
govedo
Pot uporabe:
-
intramuskularna uporaba
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Intravenska uporaba
Podatki o zdravilu
Farmacevtska oblika:
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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.
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-
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
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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.
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-
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
Ima dovoljenje za promet v:
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:
- The Veterinary Medicines Directorate
Številka dovoljenja za promet z zdravilom:
- VM 50406/4008
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
