Levacide Low Volume 7.5% Oral Solution
Active ingredient: Levamisole Hydrochloride
Form
Liquid
Species
Manufacturer
Norbrook Laboratories Limited
VMD MA No.
02000/4081
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 lu...
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Prescription required
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Levacide Low Volume 7.5% Oral Solution — SPC Details
Source: VMD Summary of Product Characteristics (SPC). Last updated 26 Mar 2026.
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. These include:
Haemonchus spp, Ostertagia spp (except inhibited Ostertagia larvae in
cattle), Nematodirus spp, Trichostrongylus spp, spp,
Oesophagostomum spp, Chabertia spp, Bunostomum spp and
Dictyocaulus spp.
mg levamisole hydrochloride per kg bodyweight. 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.
Do not mix with other products
Revised: 09 June 2010
AN: 00154/2010
treatment with organophosphorus compounds.
Revised: 09 June 2010
AN: 00154/2010
increase the risk of development of resistance and could ultimately
result in ineffective therapy:
•
class, over an extended period of time
•
weight, 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 Teladorsagia,
and Trichostrongylus species in sheep in a number of countries,
including the EU. There are reports of resistance in Haemonchus in
sheep outside the EU. Resistance to levamisole has been reported in
Teladorsagia species in cattle 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 infection in cattle, coughing may persist for a
considerable time following successful treatment with Levacide Low
Volume. This is due to tissue damage caused by the parasites.
i. Special precautions for use in animals
For oral administration only
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.
Revised: 09 June 2010
AN: 00154/2010
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. Wash
splashes from eyes and skin immediately. If irritation persists
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 this product, or sore mouth, throat or
fever occur shortly afterwards, then medical advice should be
sought immediately.
Levamisole is not affected by benzimidazole resistance.
Protect from light.
from the last treatment. Sheep may be slaughtered for human
consumption only after 21 days from the last treatment.
This product must not be used in cattle and sheep producing milk for
human consumption.
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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Other Products Containing Levamisole Hydrochloride
These products share the same active ingredient and may be suitable alternatives. Always consult your vet.
Chanaverm 7.5% Oral Solution
POM-VPSChanelle Pharmaceuticals Manufacturing Ltd
Chanaverm 7.5% Oral Solution
POM-VPSChanelle Pharmaceuticals Manufacturing Ltd
Combinex 50 mg/ml + 37.5 mg/ml Oral Suspension for Sheep
POM-VPSElanco GmbH
Combinex 50 mg/ml + 37.5 mg/ml Oral Suspension for Sheep
POM-VPSElanco GmbH
Combinex Cattle Oral Suspension
POM-VPSElanco Europe Ltd
Downland Fluke and Worm Oral Suspension
POM-VPSNorbrook Laboratories Limited
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