Boflox 100 mg/ml Solution for Injection for Cattle and Pigs
Active ingredient: Marbofloxacin
Form
Injection
Species
Manufacturer
Industrial Veterinaria SA
VMD MA No.
36547/4002
What it's used for
- treatment of acute mastitis caused by strains of marbofloxacin during the lactation period. In pigs: - treatment of Postpartum Dysgalactia Syndrome – PDS...
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Prescription required
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Boflox 100 mg/ml Solution for Injection for Cattle and Pigs — SPC Details
Source: VMD Summary of Product Characteristics (SPC). Last updated 27 Mar 2026.
marbofloxacin during the lactation period.
In pigs:
- treatment of Postpartum Dysgalactia Syndrome – PDS - (Metritis Mastitis
Agalactia syndrome), caused by bacterial strains susceptible to marbofloxacin.
AN: 00495/2025 & 00496/2025
Cattle:
Respiratory infections:
The recommended dosage is 8 mg of marbofloxacin/kg body weight (2 ml of the
veterinary medicinal product/25 kg body weight) in a single injection by
intramuscular route. If the volume to be injected is more than 20 ml, it should be
divided between two or more injection sites.
In cases of respiratory infections caused by , the
recommended dose is 2 mg of marbofloxacin/kg body weight (1 ml of the
veterinary medicinal product/50 kg body weight), in a single daily injection for 3
to 5 consecutive days, by intramuscular or subcutaneous route. The first
injection may be given by the intravenous route.
AN: 00495/2025 & 00496/2025
Acute mastitis:
- Intramuscular or subcutaneous use:
The recommended dosage is 2 mg of marbofloxacin/kg body weight (1 ml of the
veterinary medicinal product/50 kg body weight) in a single daily injection, for 3
consecutive days.
The first injection may also be given by the intravenous route.
Pig (sow):
- Intramuscular use:
The recommended dosage is 2 mg of marbofloxacin/kg body weight (1 ml of the
veterinary medicinal product/50 kg body weight) in a single daily injection, for 3
consecutive days.
To ensure a correct dosage, body weight should be determined as accurately
as possible.
In cattle and pig, the preferred injection site is the neck area.
In cattle, subcutaneous route was shown to be better tolerated locally than
intramuscular route. Therefore, the subcutaneous route is recommended in
heavy cattle.
The cap may be safely punctured up to 30 times. The user should choose the
most appropriate vial size according to the target species to treat.
fluoroquinolones (cross resistance).
Do not use in cases of hypersensitivity to the active substance, to any other
quinolone or to any of the excipients.
Very rare
(<1 animal / 10 000 animals treated,
including isolated reports):
Injection site inflammation
.
Injection site reaction
(e.g. injection site pain
, injection
site swelling
).
AN: 00495/2025 & 00496/2025
Transitory and without clinical impact, when administered via intramuscular or
subcutaneous route. After intramuscular injection inflammatory lesions may
persist for at least 12 days after injection.
When administered by intramuscular route. Transitory.
Reporting adverse events is important. It allows continuous safety monitoring of
a veterinary medicinal product. Reports should be sent, preferably via a
veterinarian, to either the marketing authorisation holder or its local
representative or the national competent authority via the national reporting
system. See the package leaflet for respective contact details.
treatment of acute forms of mastitis induced by gram-positive bacteria.
Special precautions for safe use in the target species:
Official and local antimicrobial policies should be taken into account when the
veterinary medicinal product is used.
Fluoroquinolones should be reserved for the treatment of clinical conditions
which have responded poorly, or are expected to respond poorly, to other
classes of antimicrobials.
Whenever possible, fluoroquinolones should only be used based on
susceptibility testing.
Use of the product deviating from the instructions given in the SPC may
increase the prevalence of bacteria resistant to the fluoroquinolones and may
decrease the effectiveness of treatment with other quinolones due to the
potential for cross resistance.
Special precautions to be taken by the person administering the veterinary
medicinal product to animals:
People with known hypersensitivity to (fluoro)quinolones should avoid contact
with the veterinary medicinal product.
Care should be taken to avoid accidental self-injection as it can induce a slight
irritation.
In case of accidental self-injection, seek medical advice immediately and show
the package leaflet or the label to the physician.
In case of contact with skin or eyes, rinse with plenty of water.
Wash hands after use.
Special precautions for the protection of the environment:
Not applicable.
None known.
IndicationRespiratoryMastitisDosage2 mg/kg for 3 to 5
days (i.v./i.m./s.c.)
8 mg/kg on a single
occasion (i.m.)
2 mg/kg for 3 days
(i.v./i.m./s.c.)
Meat and offal6 days3 days6 daysMilk36 hours72 hours36 hours
AN: 00495/2025 & 00496/2025
Pig (sow):
Meat and offal: 4 days
This information is sourced from the official Summary of Product Characteristics (SPC) published by the Veterinary Medicines Directorate (VMD). It is provided for informational purposes only and does not replace professional veterinary advice. Always consult your vet before administering any medication.
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Other Products Containing Marbofloxacin
These products share the same active ingredient and may be suitable alternatives. Always consult your vet.
Aurizon Ear Drops, Suspension
POM-VVetoquinol UK Ltd
Aurizon Ear Drops, Suspension
POM-VVetoquinol SA
Boflox Flavour 20 mg Tablets for Dogs and Cats
POM-VIndustrial Veterinaria SA
Boflox Flavour 20 mg Tablets for Dogs and Cats
POM-VIndustrial Veterinaria SA
Boflox Flavour 80 mg Tablets for Dogs
POM-VIndustrial Veterinaria SA
Boflox Flavour 80 mg Tablets for Dogs
POM-VIndustrial Veterinaria SA
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