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POM-V Prescription Required Companion Animal

Thyroxanil 600 Microgram Tablets for Dogs and Cats

Active ingredients: L Thyroxine Sodium, Magnesium Oxide Heavy, Magnesium Stearate

Form

Tablet

Species

Cats Dogs

Manufacturer

Le Vet Beheer B.V.

VMD MA No.

41821/4032

What it's used for

Treatment of primary and secondary hypothyroidism.

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

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Prescription required

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Clinical information

Thyroxanil 600 Microgram Tablets for Dogs and Cats — SPC Details

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

Treatment of primary and secondary hypothyroidism.
Oral use.
The recommended starting dose for dogs and cats is 20 µg levothyroxine sodium per
kg body weight per day given as a single daily dose or in two equally divided doses.
Because of variability in absorption and metabolism, the dosage may require
alterations before a complete clinical response is observed. The initial dosage and
frequency of administration are merely a starting point. Therapy has to be highly
individualised and tailored to the requirements of the individual animal especially for
cats and small dogs. For cats and small dogs, it is recommended to use the lower
strength 200 µg tablet when commencing therapy and for subsequent dose
adjustments given that more accurate dosing and dose titration is possible. The dose
should be adjusted based on clinical response and plasma thyroxine levels. In the
dog and cat, absorption of levothyroxine sodium may be affected by the presence of
food. The timing of treatment and its relation to feeding should therefore be kept
consistent from day to day. To adequately monitor therapy, trough values (just prior
to treatment) and peak values (about four hours after dosing) of plasma T4 can be
measured. In adequately dosed animals peak plasma concentration of T4 should be
in the high-normal range (approximately 30 to 47 nmol/l) and trough values should be
above approximately 19 nmol/l. If T4 levels are outside this range the levothyroxine
sodium dose can be adjusted in appropriate increments until the patient is clinically
euthyroid and serum T4 is within the reference range. The 200 µg tablets enable
adjustment of the levothyroxine dose by 50 µg increments per animal and 600 µg
tablets enable adjustment of the levothyroxine dose by 150 µg increments per
animal. Plasma T4 levels can be retested two weeks after change of dosage, but
clinical improvement is an equally important factor in determining individual dosage
and this will take four to eight weeks. When the optimum replacement dose has been
attained, clinical and biochemical monitoring may be performed every 6 – 12 months.

Revised: February 2021
AN: 00903/2020Page 4 of 7
The following table is intended as a guide to dispensing the product at approximately
the standard
day.
Administration once
daily
Administration twice
dailyBody weight
Thyroxani
l 200 µg
Thyroxa
nil 600
µg
Actual
dose
per kg
(μg)
Thyroxani
l 200 µg
Thyroxani
l 600 µg
>2.5 kg – 5
kg
20 - 10->5 kg – 7.5
kg
20 - 13.3>7.5 kg – 10
kg or
20 - 15>10 kg –
12.5 kg
20 - 16>12.5 kg –
15 kg or
24 - 20
or
>15 kg –
17.5 kg
23.3 - 20>17.5 kg –
20 kg
22.9 - 20>20 kg –
22.5 kg or
22.5 - 20>22.5 kg –
25 kg
22.2 - 20>25 kg – 30
kg or
24 - 20
or
>30 kg – 40
kg and
26.7 - 20
>40 kg – 50
kg
and
25 - 20>50 kg – 60
kg
24 - 20
= ¼ Tablet = ½ Tablet = ¾ Tablet = 1 Tablet
Tablets can be divided into halves or quarters to ensure accurate dosing. Place the
tablet on a flat surface, with its scored side facing up and the convex (rounded) side
facing the surface.

Revised: February 2021
AN: 00903/2020Page 5 of 7
Halves: press down with your thumbs on both sides of the tablet.
Quarters: press down with your thumb in the middle of the tablet.
Do not use in dogs and cats suffering from uncorrected adrenal insufficiency.
Do not use in cases of known hypersensitivity to levothyroxine sodium or to any of
the excipients.
An exacerbation of skin symptoms, with increased pruritus due to shedding of the old
epithelial cells, can occur initially. Pruritus and desquamation have been reported
very rarely in spontaneous reports.
The frequency of adverse reactions is defined using the following convention:
- very common (more than 1 in 10 animals treated displaying adverse reaction(s))
- common (more than 1 but less than 10 animals in 100 animals treated)
- uncommon (more than 1 but less than 10 animals in 1,000 animals treated)
- rare (more than 1 but less than 10 animals in 10,000 animals treated)
- very rare (less than 1 animal in 10,000 animals treated, including isolated reports).
The diagnosis of hypothyroidism should be confirmed with appropriate tests.

Special precautions for use in animals

Revised: February 2021
AN: 00903/2020Page 2 of 7
A sudden increase in demand for oxygen delivery to peripheral tissues, plus the
chronotropic effects of levothyroxine sodium, may place undue stress on a poorly
functioning heart, causing decompensation and signs of congestive heart failure.
Hypothyroid animals with concurrent hypoadrenocorticism have a decreased ability to
metabolise levothyroxine sodium and therefore an increased risk of thyrotoxicosis.
These animals should be stabilised with glucocorticoid and mineralocorticoid
treatment prior to treatment with levothyroxine sodium to avoid precipitating a
hypoadrenocortical crisis. After this, thyroid tests should be repeated, then gradual
introduction of levothyroxine is recommended (starting with 25% of the normal dose
and increasing by 25% increments every fortnight until optimal stabilisation is
achieved). Gradual introduction of therapy is also recommended for animals with
other concurrent illnesses; particularly in animals with cardiac disease, diabetes
mellitus and renal or hepatic dysfunction.
Special precautions to be taken by the person administering the veterinary medicinal
product to animals
This product contains a high concentration of levothyroxine sodium and may be
harmful when ingested, particularly for children. Pregnant women should handle this
veterinary medicinal product with caution. Levothyroxine may cause hypersensitivity
(allergy) following ingestion. Avoid skin contact with this product if you know you are
sensitized. Wash hands after handling the tablets. In the case of accidental ingestion,
seek medical advice immediately and show the package leaflet or the label to the
physician.
Any unused tablet portion(s) should be returned to the open blister, stored out of the
sight and reach of children and always be used at the next administration.
Revised: February 2021
AN: 00903/2020Page 3 of 7
A variety of drugs may impair plasma or tissue binding of the thyroid hormones or
alter thyroid hormone metabolism (e.g. barbiturates, antacids, anabolic steroids,
diazepam, furosemide, mitotane, phenylbutazone, phenytoin, propranolol, large
doses of salicylates and sulphonamides). When treating animals that are receiving
concurrent medication the properties of these drugs should be taken into
consideration.
Oestrogens may increase thyroid requirements.
Ketamine may cause tachycardia and hypertension when used in patients receiving
thyroid hormones.
The effect of catecholamines and sympathomimetics is increased by levothyroxine.
An increase in the dosage of digitalis may be necessary in a patient that had
previously compensated congestive heart failure and that is placed on thyroid
hormone supplementation. Following treatment of hypothyroidism in patients with
concurrent diabetes, careful monitoring of diabetic control is recommended.
Most patients on chronic high-dose, daily glucocorticoid therapy will have very low or
undetectable serum T4 concentrations, as well as subnormal T3 values.
Do not store above 25°C.
Keep the blisters in the outer carton in order to protect from light.
Not applicable.
5.

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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