MARBOCYL 100 MG/ML, SOLUTION FOR INJECTION FOR CATTLE AND PIGS
MARBOCYL 100 MG/ML, SOLUTION FOR INJECTION FOR CATTLE AND PIGS
Authorised
- Marbofloxacin
Product identification
Medicine name:
MARBOCYL 100 MG/ML, SOLUTION FOR INJECTION FOR CATTLE AND PIGS
Active substance:
- Marbofloxacin
Target species:
-
Cattle
-
Pig
Route of administration:
-
Intramuscular use
-
Subcutaneous 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
-
Meat and offal6dayIndication : Respiratory
Dosage : 2 m/kg for 3 to 5 days (IV/IM/SC) -
Milk36hourIndication : Mastitis
Dosage : 2mg/kg for 3 days (IV/IM/SC) -
Meat and offal6dayIndication : Mastitis
Dosage : 2mg/kg for 3 days (IV/IM/SC) -
Milk72hourIndication : Respiratory
Dosage : 8 mg/kg on a single occasion (IM) -
Meat and offal3dayIndication : Respiratory
Dosage : 8 mg/kg on a single occasion (IM) -
Milk36hourIndication : Respiratory
Dosage : 2 m/kg for 3 to 5 days (IV/IM/SC)
-
-
Pig
-
Meat and offal4day
-
-
-
Subcutaneous use
-
Cattle
-
Meat and offal6dayIndication : Respiratory
Dosage : 2 m/kg for 3 to 5 days (IV/IM/SC) -
Milk36hourIndication : Mastitis
Dosage : 2mg/kg for 3 days (IV/IM/SC) -
Meat and offal6dayIndication : Mastitis
Dosage : 2mg/kg for 3 days (IV/IM/SC) -
Milk72hourIndication : Respiratory
Dosage : 8 mg/kg on a single occasion (IM) -
Meat and offal3dayIndication : Respiratory
Dosage : 8 mg/kg on a single occasion (IM) -
Milk36hourIndication : Respiratory
Dosage : 2 m/kg for 3 to 5 days (IV/IM/SC)
-
-
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
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application - Known active substance (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Vetoquinol
Marketing authorisation date:
Manufacturing sites for batch release:
- Vetoquinol Biowet Sp. z o.o.
- Vetoquinol S.A.
Responsible authority:
- Federal Agency For Medicines And Health Products
Authorisation number:
- BE-V198511
Date of authorisation status change:
Reference member state:
-
France
Procedure number:
- FR/V/0107/001
Concerned member states:
-
Austria
-
Belgium
-
Germany
-
Greece
-
Italy
-
Luxembourg
-
Portugal
-
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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Labelling
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Combined File of all Documents
English (PDF)
Download Published on: 14/03/2026