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
Awtorizzat
- Metamizole sodium monohydrate
- Hyoscine butylbromide
Identifikazzjoni tal-prodott
Isem tal-mediċina:
SYMPAGESIC 500 MG/ML + 4 MG/ML SOLUTION FOR INJECTION FOR HORSES, CATTLE, PIGS AND DOGS
Sympagesic 500+4 mg/ml injektionsvæske, opløsning
Speċi li fuqhom ser jintuża l-prodott:
Metodu ta’ amministrazzjoni:
-
Użu għal ġol-muskoli
-
Użu għal ġol-vini
Dettalji tal-prodott
Forma farmaċewtika:
-
Soluzzjoni għall-injezzjoni
Withdrawal period by route of administration:
-
Użu għal ġol-muskoli
-
Cattle
-
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
-
-
Użu għal ġol-vini
-
Cattle
-
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
-
Kodiċi veterinarju anatomiku terapewtiku kimiku (ATCvet):
- QA03DB04
Status tal-awtorizzazzjoni:
-
Valid
Tagħrif addizzjonali
Id-detentur tal-awtorizzazzjoni għat-tqegħid fis-suq:
- Dechra Regulatory B.V.
Marketing authorisation date:
Siti ta’ manifattura b’rilaxx tal-lott:
- Genera d.d.
Awtorità responsabbli:
- Danish Medicines Agency
Numru tal-awtorizzazzjoni:
- 61295
Data tal-bidla fl-istatus tal-awtorizzazzjoni:
Numru tal-proċedura:
- FR/V/0354/001
Stati Membri Kkonċernati:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Dokumenti
Sommarju tal-karatteristiċi tal-prodott
Dan id-dokument ma jeżistix f'dan il-lingwa (Malti). Tista 'ssibha f'lingwa oħra hawn taħt.
Danish (PDF)
Ippubblikat fuq: 29/06/2023
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