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
-
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.
-
-
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:
- Health Products Regulatory Authority
Številka dovoljenja za promet z zdravilom:
- VPA22622/033/001
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
