MARFLOQUIN 100 MG/ML SOLUTION FOR INJECTION FOR BOVINES AND PIGS (SOWS)
MARFLOQUIN 100 MG/ML SOLUTION FOR INJECTION FOR BOVINES AND PIGS (SOWS)
Authorised
- Marbofloxacin
Product identification
Medicine name:
MARFLOQUIN 100 MG/ML SOLUTION FOR INJECTION FOR BOVINES AND PIGS (SOWS)
Marfloquin 100 mg/ml Oplossing voor injectie
Marfloquin 100 mg/ml Solution injectable
Marfloquin 100 mg/ml Injektionslösung
Active substance:
- Marbofloxacin
Target species:
-
Cattle
-
Pig (sow)
Route of administration:
-
Intramuscular use
-
Subcutaneous use
-
Intravenous use
Product details
Active substance and strength:
-
Marbofloxacin100.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Cattle
-
Milk36hour2 mg/kg single daily injection, for 3 days
-
Meat and offal6day2 mg/kg single daily injection, for 3 days
-
Milk72hour8 mg/kg single dose
-
Meat and offal3day8 mg/kg single dose
-
-
Pig (sow)
-
Meat and offal4day
-
-
-
Subcutaneous use
-
Cattle
-
Meat and offal6day2 mg/kg single daily injection, for 3 days
-
Milk36hour2 mg/kg single daily injection, for 3 days
-
-
-
Intravenous use
-
Cattle
-
Meat and offal6day2 mg/kg single daily injection, for 3 days (the first injection may also be given by the intravenous route too)
-
Milk36hour2 mg/kg single daily injection, for 3 days (the first injection may also be given by the intravenous route too)
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01MA93
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Belgium
Available in:
-
Belgium
Package description:
- Box of one 50 ml solution bottle for injection
- Box of one 250 ml solution bottle for injection
- Box of one 100 ml solution bottle for injection
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Generic application (Article 13(1) of Directive No 2001/82/EC)
Marketing authorisation holder:
- KRKA tovarna zdravil d.d. Novo mesto
Marketing authorisation date:
Manufacturing sites for batch release:
- KRKA tovarna zdravil d.d. Novo mesto
- Virbac
Responsible authority:
- Federal Agency For Medicines And Health Products
Authorisation number:
- BE-V392953
Date of authorisation status change:
Reference member state:
-
France
Procedure number:
- FR/V/0223/002
Concerned member states:
-
Austria
-
Belgium
-
Czechia
-
Germany
-
Greece
-
Hungary
-
Italy
-
Latvia
-
Lithuania
-
Portugal
-
Slovakia
-
Spain
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
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Package Leaflet
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Combined File of all Documents
English (PDF)
Download Published on: 11/06/2025
Labelling
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