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
Pooblaščeno
- Metamizole sodium monohydrate
- Hyoscine butylbromide
Identifikacija zdravila
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:
-
Raztopina za injiciranje
Withdrawal period by route of administration:
-
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
-
-
Dog
-
-
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.
-
-
Dog
-
Anatomsko-terapevtsko-kemična veterinarska oznaka (ATCvet):
- QA03DB04
Pravni status za dobavo / izdajo zdravila:
-
Zdravilo, ki se izdaja na veterinarski recept
Status dovoljenja:
-
Valid
Dodatne informacije
Imetnik dovoljenja za promet z zdravilom:
- Dechra Regulatory B.V.
Marketing authorisation date:
Proizvodna mesta, odgovorna za sproščanje serij:
- GENERA d.d.
Pristojni organ:
- Health Products Regulatory Authority
Številka dovoljenja :
- VPA22622/033/001
Datum spremembe statusa dovoljenja:
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
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