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POM-VPS Prescription Required

Levacide 7.5% Solution for Injection for Cattle and Sheep

Active ingredient: Levamisole Hydrochloride

Form

Injection

Species

Cattle Sheep

Manufacturer

Norbrook Laboratories Limited

VMD MA No.

02000/4049

What it's used for

A broad spectrum anthelmintic for use in the treatment and control of nematode infections. It should be used in cases of parasitic gastro-enteritis and lun...

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

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Paying less for Levamisole Hydrochloride

  1. 1

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    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

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Clinical information

Levacide 7.5% Solution for Injection for Cattle and Sheep — SPC Details

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

A broad spectrum anthelmintic for use in the treatment and control of
nematode infections. It should be used in cases of parasitic gastro-enteritis
and lungworm disease caused by mature and developing immature forms of
those organisms sensitive to treatment with levamisole hydrochloride.
Administer by subcutaneous injection at a rate of 7.5 mg Levamisole per kg
bodyweight. Usual aseptic precautions should be observed. Cattle should be
dosed at a rate of 1 ml of product per 10 kg bodyweight and sheep at a rate of
0.5 ml per 5 kg bodyweight. To ensure administration of a correct dose,
bodyweight should be determined as accurately as possible; accuracy of the
dosing device should be checked.
Divide large doses between two or more injection sites. In order to minimise
the risk of infection, needles should be changed frequently.
Do not mix with any other products before administration except if premixing
is done by a veterinary surgeon or a pharmacist.
Animals must not be treated within a period of 14 days before or after
treatment with organophosphorus compounds.
Although normally non-irritant, the product may occasionally cause local
reaction at the site of injection. This should resolve naturally in a short period
of time.
Care should be taken to avoid the following practices because they increase
the risk of development of resistance and could ultimately result in ineffective
therapy:
•
an extended period of time.

Revised: July 2010
(ATC vet code amended)
•
misadministration of the product, or lack of calibration of the dosing
device (if any).
Suspected clinical cases of resistance to anthelmintics should be further
investigated using appropriate tests (e.g. Faecal Egg Count Reduction Test).
Where the results of the test(s) strongly suggest resistance to a particular
anthelmintic, an anthelmintic belonging to another pharmacological class and
having a different mode of action should be used.
Resistance to levamisole has been reported in , and
Trichostrongylus species in sheep in a number of countries, including the EU.
There are reports of resistance in in sheep outside the EU.
Resistance to levamisole has been reported in
in developed countries such as New Zealand. Therefore the use of this
product should be based on local (regional, farm) epidemiological information
about susceptibility of nematodes and recommendations on how to limit
further selection for resistance to anthelmintics.
In cases of lungworm infections, coughing may persist for a considerable time
following successful treatment due to tissue damage caused by the parasite.

i. Special precautions for use in animals
Care should be taken to estimate accurately the liveweight of animals to
be treated. After treatment animals should be moved to clean pasture in
order to prevent re-infection.
Veterinary advice should be sought:
a) On appropriate dosing programmes and stock management to achieve
adequate parasite control, and to reduce the likelihood of anthelmintic
resistance developing.
b) If the product does not achieve the desired clinical effect since other
diseases, nutritional disturbances or anthelmintic resistance might be
involved.
ii. Special precautions to be taken by the person administering the veterinary
medicinal product to animals
Do not eat, drink or smoke when using this product. Care should be taken
to avoid accidental self-injection: may cause irritation at site of injection.
Wash splashes from eyes and skin immediately. If irritation persist, seek
medical advice. Remove any contaminated clothing immediately. Wash
hands and exposed skin after handling this product and before meals.
Levamisole can cause idiosyncratic reactions and serious blood disorders
in a very small number of people. If symptoms such as dizziness,
nausea, vomiting or abdominal discomfort are experienced when using

Revised: July 2010
(ATC vet code amended)
this product, or sore mouth, throat or fever occur shortly afterwards, then
medical advice should be sought immediately.
Levamisole activity is not affected by benzimidazole resistance.
Do not store above 25C.
Protect from light.
In order to minimise the risk of infection, needles should be changed as
frequently as possible.
Following withdrawal of the first dose, use the product within 28 days.
Cattle may be slaughtered for human consumption only after 28 days from the
last treatment. Sheep may be slaughtered for human consumption only after
15 days from the last treatment.
This product must not be used in cattle and sheep producing milk for human
consumption.

Revised: July 2010
(ATC vet code amended)
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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