ORBENIN EDC, 600 mg intramaminė suspensija galvijams
ORBENIN EDC, 600 mg intramaminė suspensija galvijams
Authorised
- Cloxacillin
Product identification
Medicine name:
ORBENIN EDC, 600 mg intramaminė suspensija galvijams
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 offal28day
-
Milk96hour96 val. po veršiavimosi, jei gydyta likus ne mažiau kaip 42 paroms iki veršiavimosi, 46 paros (42 paros plius 96 val.) po vaisto naudojimo, jei karvė veršiavosi nepraėjus 42 paroms po gydymo
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ51CF02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Lithuania
Package description:
- Available only in Lithuanian
- Available only in Lithuanian
- Available only in Lithuanian
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis reviewed according to Acquis communautaire
Marketing authorisation holder:
- Zoetis Belgium
Marketing authorisation date:
Manufacturing sites for batch release:
- Zoetis Belgium
Responsible authority:
- State Food And Veterinary Service
Authorisation number:
- LT/2/00/1072/001-003
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
This document does not exist in this language (English). You can find it
in another language below.
Lithuanian (PDF)
Published on: 3/09/2024
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