BOVIX MICROCLOX EDC, 600 mg Intramammary Suspension
BOVIX MICROCLOX EDC, 600 mg Intramammary Suspension
Authorised
- Cloxacillin
Product identification
Medicine name:
BOVIX MICROCLOX EDC, 600 mg Intramammary Suspension
Active substance:
- Cloxacillin
Target species:
-
Cattle (dairy cow at drying-off)
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 (dairy cow at drying-off)
-
Meat and offalno withdrawal periodMeat and offal: zero days
-
Milk48hour- if calving occurs at least 42 days after treatment: 48 hours post calving. - if calving occurs less than 42 days after treatment: 44 days after last treatment.
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ51CF02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Belgium
Package description:
- Cardboard box with 12 syringes x 3.6 g of veterinary medicinal product and wipes.
- Cardboard box with 24 syringes x 3.6 g of veterinary medicinal product and wipes.
- Cardboard box with 60 syringes x 3.6 g of veterinary medicinal product and wipes.
- Cardboard box with 120 syringes x 3.6 g of veterinary medicinal product and wipes.
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Hybrid application – bioavailability studies cannot be used to demonstrate bioequivalence (Article 19(1)(b) of Regulation (EU) 2019/6)
Marketing authorisation holder:
- Kernfarm B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Crida Pharm S.R.L.
Responsible authority:
- Federal Agency For Medicines And Health Products
Authorisation number:
- BE-V663933
Date of authorisation status change:
Reference member state:
-
Netherlands
Procedure number:
- NL/V/0416/001
Concerned member states:
-
Belgium
-
France
-
Germany
-
Italy
-
Poland
-
Spain
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Package Leaflet
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Labelling
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Summary of Product Characteristics
This document does not exist in this language (English). You can find it in another language below.
Combined File of all Documents
English (PDF)
Download Published on: 9/01/2025
Updated on: 13/03/2026
English (PDF)
Published on: 14/03/2026
