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
Autoriseret
- Metamizole sodium monohydrate
- Hyoscine butylbromide
Produktidentifikation
Lægemiddelnavn:
SYMPAGESIC 500 MG/ML + 4 MG/ML SOLUTION FOR INJECTION FOR HORSES, CATTLE, PIGS AND DOGS
Sympagesic 500 mg/ml + 4 mg/ml ενέσιμο διάλυμα για άλογα, βοοειδή, χοίρους και σκύλους
Dyreart:
-
Kvæg
-
Svin
-
Hund
-
Hest
-
Hoppe
Administrationsvej:
-
Intramuskulær anvendelse
-
Intravenøs anvendelse
Produktoplysninger
Lægemiddelform:
-
Injektionsvæske, opløsning
Tilbageholdelsestid efter administrationsrute:
-
Intramuskulær anvendelse
-
Kvæg
-
Meat and offal28dag
-
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.
-
-
Svin
-
Meat and offal15dag
-
-
-
Intravenøs anvendelse
-
Kvæg
-
Meat and offal18dag
-
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.
-
-
Svin
-
Meat and offal15dag
-
-
Hest
-
Meat and offal15dag
-
-
Hoppe
-
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.
-
-
Anatomisk terapeutisk kemisk veterinær (ATCvet) kode:
- QA03DB04
Godkendelsesstatus:
-
Gyldig
Yderligere oplysninger
Indehaver af markedsføringstilladelsen:
- Dechra Regulatory B.V.
Dato for markedsføringstilladelse:
Fremstillere ansvarlige for batchfrigivelse:
- Genera d.d.
Ansvarlig myndighed:
- Veterinary Services, Ministry Of Agriculture, Natural Resources And Environment
Markedsføringstilladelsesnummer:
- CY00738V
Dato for ændring af godkendelsesstatus:
Procedurenummer:
- FR/V/0354/001
Berørte medlemsstater:
Indberetninger om formodede bivirkninger på veterinærlægemidler: www.adrreports.eu/vet
Dokumenter
Produktresumé
Dette dokument findes ikke på dette sprog (dansk). Du kan finde det på et andet sprog nedenfor.
Greek (PDF)
Udgivet den: 15/06/2022
