Orbenin Extra DC 600 mg intramamálna suspenzia pre hovädzí dobytok
Orbenin Extra DC 600 mg intramamálna suspenzia pre hovädzí dobytok
Authorised
- Cloxacillin hemibenzathine
Product identification
Medicine name:
Orbenin Extra DC 600 mg intramamálna suspenzia pre hovädzí dobytok
Active substance:
- Cloxacillin hemibenzathine
Target species:
-
Cattle (dairy cow at drying-off)
Route of administration:
-
Intramammary use
Product details
Active substance and strength:
-
Cloxacillin hemibenzathine1530.80/milligram(s)1.00Syringe
Pharmaceutical form:
-
Intramammary suspension
Withdrawal period by route of administration:
-
Intramammary use
-
Cattle (dairy cow at drying-off)
-
Meat and offal28day
-
Milk4dayMlieko: Liek sa nesmie používať v laktácii, ale výhradne v období zasušenia, a to najneskôr 42 dní pred pôrodom. Ochranná lehota pre mlieko je 4 dni po pôrode. Ak k oteleniu dôjde skôr, ochranná lehota sa vypočíta tak, že k termínu aplikácie sa pripočíta 46 dní (t.j. 42+4 dni).
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ51CF02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Slovakia
Available in:
-
Slovakia
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
- Zoetis Ceska Republika s.r.o.
Marketing authorisation date:
Manufacturing sites for batch release:
- Haupt Pharma Latina S.r.l.
Responsible authority:
- Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
- 96/257/91-S
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
This document does not exist in this language (English). You can find it in another language below.
Slovak (PDF)
Published on: 14/10/2025
