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POM-V Prescription Required Companion Animal

Enrotron 25 mg/ml Solution for Injection for Dogs, Cats, Rodents, Reptiles and Ornamental Birds

Active ingredient: Enrofloxacin

Form

Injection

Species

Cats Dogs Ornamental Birds Reptiles Rodents

Manufacturer

aniMedica GmbH

VMD MA No.

24745/4029

What it's used for

Dogs Treatment of infections of the alimentary, respiratory and urogenital tracts (including prostatitis, adjunctive antibiotic therapy for pyometra), skin...

Full indications, dosage and side effects ↓
View official SPC (PDF)

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Prescription required

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Clinical information

Enrotron 25 mg/ml Solution for Injection for Dogs, Cats, Rodents, Reptiles and Ornamental Birds — SPC Details

Source: VMD Summary of Product Characteristics (SPC). Last updated 26 Mar 2026.

Dogs
Treatment of infections of the alimentary, respiratory and urogenital tracts (including
prostatitis, adjunctive antibiotic therapy for pyometra), skin and wound infections,
otitis (externa/media) caused by enrofloxacin susceptible strains of: Staphylococcus
spp., Escherichia coli, Pasteurella spp., Klebsiella ., Bordetella spp.,
Pseudomonas spp. and Proteus spp
Cats
Treatment of infections of the alimentary, respiratory and urogenital tracts (as
adjunctive antibiotic therapy for pyometra), skin and wound infections, caused by
enrofloxacin susceptible strains of: Staphylococcus spp
spp., Klebsiella spp., Bordetella spp., Pseudomonas sppand Proteus spp.

Revised: February 2019
AN: 01476/2018
Rodents, Reptiles and Ornamental birds: Treatment of infections of the alimentary
and respiratory tracts where clinical experience, if possible, supported by
susceptibility testing of the causal organism, indicates enrofloxacin as the substance
of choice.
Subcutaneous or intramuscular use.
Repeated injections should be made at different injection sites.
To ensure a correct dosage, body weight (bw) should be determined as accurately as
possible to avoid underdosing.
Dogs and cats
5 mg of enrofloxacin/kg bw, corresponding to 1 ml/5 kg bw, daily by subcutaneous
injection for up to 5 days.
Treatment may be initiated with injectable product and maintained with enrofloxacin
tablets. Duration of treatment should be based on the duration of treatment approved
for the appropriate indication in the product information of the tablet product.
Rodents
10 mg/kg bw, corresponding to 0.4 ml/kg bw, once daily by subcutaneous injection
for 5 to 10 consecutive days. If necessary, depending on the severity of clinical signs,
this dosage can be doubled.

Revised: February 2019
AN: 01476/2018
Reptiles
Reptiles are ectothermic, relying on external heat sources to maintain their body
temperature at the optimum level for correct function of all body systems. Metabolism
of substances and activity of the immune system are, thus, critically dependent on
the body temperature. Therefore, the veterinarian must be aware of the correct
temperature requirements of the respective reptile species and the hydration status
of the individual patient. Furthermore, it has to be considered that large differences
exist in the pharmacokinetic behaviour of enrofloxacin among different species, which
additionally will influence the decision about the correct dosage of Enrotron 25 mg/ml
Solution for injection.
Therefore, the recommendations made here can only be used as a starting point for
individual dose setting. 5–10 mg/kg bw, corresponding to 0.2–0.4 ml/kg bw, once
daily by intramuscular injection for 5 consecutive days.
An extension of the treatment interval to 48 hours may be necessary in individual
cases. In complicated infections, higher dosages and longer treatment courses may
be necessary. The presence of the renal portal system in reptiles means it is prudent
to administer substances in the front half of the body wherever possible.
Ornamental birds
20 mg/kg bw, corresponding to 0.8 ml/kg bw, once daily by intramuscular injection for
5 to 10 consecutive days. In case of complicated infections higher doses may be
necessary.
The use of a 0.5 ml (100 unit) insulin syringe should be considered for administration
of the small volumes required by some species of small animals (mice, gerbils etc.)
Treatment may be initiated with the injection and maintained with an enrofloxacin
containing oral solution.
Do not use in dogs less than 1 year of age or in exceptionally large breeds of dog
with a longer growth period under 18 months of age.
Do not use for cats less than 8 weeks of age.
Do not use in cases of known hypersensitivity to fluoroquinolones or to any of the
excipients.
Do not use in animals that are epileptic or suffer from seizures since enrofloxacin
may cause CNS stimulation.
Do not use for prophylaxis.
Do not use when resistance / cross resistance to (fluoro)quinolones is known to
occur. Refer to section 4.5.
In dogs enrofloxacin may affect articular cartilage during the period of rapid growth.
Occasionally skin reactions have been seen after administration to kennelled
greyhounds.
Local tissue reactions may occasionally occur at the injection site. Normal sterile
precautions should be taken.
Rodents, reptiles and ornamental birds: Muscle bruising after injection in reptiles
and birds has been reported occasionally.
In dogs enrofloxacin may affect the articular cartilage during the period of rapid
growth.

Special precautions for use in animals
Official and local antimicrobial policies should be taken into account when the 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.
Enrofloxacin should be used with caution in epileptic animals or animals affected by
renal dysfunction.
Special precautions to be taken by the person administering the veterinary medicinal
product to animals
The product is an alkaline solution. Direct contact with skin should be avoided due to
sensitisation, contact dermatitis and possible hypersensitivity reactions to
(fluoro)quinolones. Wear gloves. In case of eye or skin contact, rinse immediately
with water. Do not eat, drink or smoke whilst handling the product.
Care should be taken to avoid accidental self-injection. If accidental injection occurs,
seek medical advice immediately and show the package leaflet or the label to the
physician.

Revised: February 2019
AN: 01476/2018
Antagonistic effects due to concurrent administration of macrolides and tetracyclines
may occur. Enrofloxacin may interfere with the metabolism of theophylline,
decreasing theophylline clearance resulting in increased plasma levels of
theophylline.
Care should be taken during the concomitant use of flunixin and enrofloxacin in dogs
to avoid adverse drug reactions. The decrease in drug clearances as a result of co-
administration of flunixin and enrofloxacin indicates that these substances interact
during the elimination phase. Thus, in dogs, the co-administration of enrofloxacin and
flunixin increased the AUC and the elimination half-life of flunixin and increased the
elimination half-life and reduced the Cmax of enrofloxacin.
Keep the vial in the outer carton in order to protect from light.
Excipients
1-Butanol 30.0 mg
For the full list of excipients, see section

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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