ORBENIN EXTRA DRY COW
ORBENIN EXTRA DRY COW
Authorised
- Cloxacillin
Product identification
Medicine name:
ORBENIN EXTRA DRY COW
Active substance:
- Cloxacillin
Target species:
-
Cattle (dry cow)
Route of administration:
-
Intramammary use
Product details
Active substance and strength:
-
Cloxacillin600.00/milligram(s)1.00Syringe
Pharmaceutical form:
-
Intramammary suspension
Withdrawal period by route of administration:
-
Intramammary use
-
Cattle (dry cow)
-
Meat and offal28dayAnimalele destinate consumului uman nu vor fi sacrificate în cursul tratamentului. Bovinele pot fi sacrificate după 28 zile de la ultimul tratament.
-
Milk96hourNu se va administra la vacile a căror perioadă de repaus mamar este de 42 de zile sau mai puţin. Laptele pentru consum uman poate fi utilizat doar la 96 de ore de la fătare. Dacă fătarea intervine în cele 42 de zile după ultimul tratament,laptele poate fi dat în consum uman numai după trecerea celor 42 de zile plus încă cele 96 de ore adiţionale.
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ51CF02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Romania
Available in:
-
Romania
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Complete application (stand-alone) - Directive No 2001/82/EC
Marketing authorisation holder:
- Zoetis Belgium
Marketing authorisation date:
Manufacturing sites for batch release:
- Haupt Pharma Latina S.r.l.
Responsible authority:
- Institute For Control Of Biological Products And Veterinary Medicines
Authorisation number:
- 130167
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Combined File of all Documents
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Romanian (PDF)
Published on: 16/04/2025
