LABIXXIN 100MG/ML SOLUTION FOR INJECTION FOR CATTLE, PIGS AND SHEEP
LABIXXIN 100MG/ML SOLUTION FOR INJECTION FOR CATTLE, PIGS AND SHEEP
Autoriseret
- Tulathromycin
Produktidentifikation
Lægemidlets navn:
LABIXXIN 100MG/ML SOLUTION FOR INJECTION FOR CATTLE, PIGS AND SHEEP
Labixxin, 100 mg/mL, otopina za injekciju, za goveda, svinje i ovce
Aktiv substans:
- Kun tilgængelig på English
Dyrearter:
-
Svin
-
Kvæg
-
Får
Administrationsvej:
-
Intramuskulær anvendelse
-
Subkutan anvendelse
Produktoplysninger
Aktiv substans / Styrke:
-
Kun tilgængelig på English100.00milligram(s)/millilitre1.00millilitre(s)
Lægemiddelform:
-
Injektionsvæske, opløsning
Withdrawal period by route of administration:
-
Intramuskulær anvendelse
- Svin
-
Meat and offal13day
-
- Kvæg
-
Meat and offal22day
-
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.
-
- Får
-
Meat and offal16day
-
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.
-
-
Subkutan anvendelse
- Svin
-
Meat and offal13day
-
- Kvæg
-
Meat and offal22day
-
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.
-
- Får
-
Meat and offal16day
-
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:
- QJ01FA94
Godkendelsesstatus:
-
Valid
Yderligere oplysninger
Indehaver af markedsføringstilladelsen:
- Labiana Life Sciences S.A.
Marketing authorisation date:
Produktionssteder for batchfrigivelse:
- Labiana Life Sciences S.A.
Ansvarlig myndighed:
- Ministry Of Agriculture Veterinary And Food Safety Directorate
Markedsføringstilladelsesnummer:
- UP/I-322-05/23-01/775
Dato for ændring af godkendelsesstatus:
Procedurenummer:
- ES/V/0423/001
Disse oplysninger foreligger ikke for dette produkt.
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Dokumenter
Produktresumé
Dette dokument findes ikke på dette sprog (dansk). Du kan finde det på et andet sprog nedenfor.
Croatian (PDF)
Udgivet den: 5/01/2024
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