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POM-V Prescription Required Companion Animal

Animeloxan 1.5 mg/ml Oral Suspension for Dogs

Active ingredient: Meloxicam

Form

Liquid

Species

Dogs

Manufacturer

aniMedica GmbH

VMD MA No.

24745/3000

What it's used for

AN: 03288/2022Page 2 of 7

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

The prescription itself has a price. See what practices near you charge for a consultation and the written prescription fee.

Paying less for Meloxicam

  1. 1

    Ask your vet for a written prescription

    They must provide one on request. Under the CMA Order the fee is capped at £21 from 2027.

  2. 2

    Fill it at a registered online retailer

    The CMA found online pharmacies 50–60% cheaper than practice dispensing on common medicines — typically £200–£300 a year.

Prescription required

Your vet must provide a written prescription on request. You can then purchase from any licensed online retailer.

Clinical information

Animeloxan 1.5 mg/ml Oral Suspension for Dogs — SPC Details

Source: VMD Summary of Product Characteristics (SPC). Last updated 27 Mar 2026.

AN: 03288/2022Page 2 of 7
To be administered mixed with food or directly into the mouth.
Initial treatment is a single dose of 0.2 mg meloxicam/kg body weight on the first day.
Treatment is to be continued once daily by oral administration (at 24-hour intervals)
at a maintenance dose of 0.1 mg meloxicam/kg body weight (equivalent to 0,07
ml/kg).
Particular care should be taken with regard to the accuracy of dosing.
The suspension can be given using the measuring syringe provided in the package.
The syringe provided allows dosing for dogs with a body weight of 2.5 – 45 kg. For
dosing for dogs with a body weight of less than 2.5 kg, a syringe with a smaller
volume (0.5 ml, 1 ml) must be used. The syringe fits onto the bottle and has a kg-
body weight scale which corresponds to the maintenance dose (i.e. 0.1 mg
meloxicam/kg body weight corresponds to 0,07 ml/kg bodyweight). Thus for the first
day, twice the maintenance volume will be required.
AN: 03288/2022Page 4 of 7
Shake bottle well.
Push down and
unscrew bottle
top. Attach the
dosing syringe to
the bottle by
gently pushing the
end onto the top
of the bottle.
Turn the
bottle/syringe
upside down. Pull
the plunger out
until the line on
the plunger
corresponds to
your dog’s
bodyweight in
kilograms
Turn the bottle right
way up and with a
twisting movement
separate the dosing
syringe from the
bottle
Empty the
contents of the
syringe onto the
food by pushing
the plunger in or
directly into the
mouth.
A clinical response is normally seen within 3 - 4 days. Treatment should be
discontinued after 10 days at the latest if no clinical improvement is apparent.
For longer term treatment, once clinical response has been observed (after ≥ 4 days),
the dose of the veterinary medicinal product can be adjusted to the lowest effective
individual dose reflecting that the degree of pain and inflammation associated with
chronic musculo-skeletal disorders may vary over time.
Avoid introduction of contamination during use.
Do not use in pregnant or lactating animals.
Do not use in animals suffering from gastrointestinal disorders such as irritation and
haemorrhage, impaired hepatic, cardiac or renal function and haemorrhagic
disorders.
Do not use in cases of hypersensitivity to the active substance or to any of the
excipients.
Do not use in dogs less than 6 weeks of age.
Dog:
Undetermined frequency
(cannot be estimated from the
available data):
Appetite loss
, vomiting
, diarrhoea
, blood in
faeces
1,2
, apathy
1
These typical adverse drug reactions of NSAIDs occur occasionally and generally
within the first treatment week and are in most cases transient and disappear
following termination of the treatment but in very rare cases may be serious or fatal.
occult
AN: 03288/2022Page 3 of 7
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 also the package leaflet
for respective contact details.
None.

Special precautions for safe use in the target species:
If adverse reactions occur, treatment should be discontinued and the advice of a
veterinarian should be sought.
Avoid use in any dehydrated, hypovolaemic or hypotensive animal, as there is a
potential risk of increased renal toxicity.
In case of prolonged use, monitoring during treatment should be carried out.
Special precautions to be taken by the person administering the veterinary medicinal
product to animals:
People with known hypersensitivity to NSAIDs should avoid contact with the
veterinary medicinal product.
In case of accidental ingestion, seek medical advice immediately and show the
package leaflet or the label to the physician.
Special precautions for the protection of the environment:
Not applicable.
Other NSAIDs, diuretics, anticoagulants, aminoglycoside antibiotics and substances
with high protein binding may compete for binding and thus lead to toxic effects.
Meloxicam must not be administered in conjunction with other NSAIDs or
glucocorticosteroids.
Pre-treatment with anti-inflammatory substances may result in additional or increased
adverse effects and accordingly a treatment-free period with such drugs should be
observed for at least 24 hours before commencement of treatment. The treatment-
free period, however, should take into account the pharmacokinetic properties of the
veterinary medicinal products used previously.
Meloxicam may antagonise the antihypertensive effects of ACE inhibitors.
This veterinary medicinal product does not require any special storage conditions.
Not applicable.

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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