CADOREX 300 mg/ml Solution for injection for cattle, pigs and sheep
CADOREX 300 mg/ml Solution for injection for cattle, pigs and sheep
Authorised
- Florfenikols
Produktidentifikation
Lægemidlets navn:
CADOREX 300 mg/ml Solution for injection for cattle, pigs and sheep
Cadorex 300 mg/ml, ενέσιμο διάλυμα για βοοειδή, πρόβατα και χοίρους
Aktiv substans:
- Kun tilgængelig på English
Dyrearter:
-
Kvæg
-
Får
-
Svin
Administrationsvej:
-
Intramuskulær anvendelse
-
Subkutan anvendelse
Produktoplysninger
Aktiv substans / Styrke:
-
Kun tilgængelig på English300.00milligram(s)1.00millilitre(s)
Lægemiddelform:
-
Injektionsvæske, opløsning
Withdrawal period by route of administration:
-
Intramuscular use
- Kvæg
-
Meat and offalno withdrawal periodMeat and offal: IM: 30 dAYS / SC: 44 Days
-
Milkno withdrawal periodMilk: Not authorised for use in animals producing milk for human consumption.
-
- Får
-
Meat and offalno withdrawal periodMeat and offal: im 39 Days
-
Milkno withdrawal periodMilk: Not authorised for use in animals producing milk for human consumption.
-
- Svin
-
Meat and offalno withdrawal periodIM 18 days
-
-
Subcutaneous use
- Kvæg
-
Meat and offalno withdrawal periodMeat and offal: IM: 30 dAYS / SC: 44 Days
-
Milkno withdrawal periodMilk: Not authorised for use in animals producing milk for human consumption.
-
- Får
-
Meat and offalno withdrawal periodMeat and offal: im 39 Days
-
Milkno withdrawal periodMilk: Not authorised for use in animals producing milk for human consumption.
-
- Svin
Anatomisk terapeutisk kemisk veterinær (ATCvet) kode:
- QJ01BA90
Godkendelsesstatus:
-
Valid
Authorised in:
-
Cyprus
-
European Union
Available in:
-
Cyprus
Yderligere oplysninger
Indehaver af markedsføringstilladelsen:
- Livisto Int'l S.L.
Markedsføringstilladelse udstedt:
Produktionssteder for batchfrigivelse:
- Industrial Veterinaria S.A.
- Animedica GmbH
Ansvarlig myndighed:
- Ministry Of Agriculture Rural Development And Environment
Markedsføringstilladelsesnummer:
- CY00638V
Dato for ændring af godkendelsesstatus:
Procedurenummer:
- ES/V/0246/001
Berørte medlemsstater:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Dokumenter
Combined File of all Documents
Published:
Greek (PDF)
Download
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