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POM-VPS Prescription Required

Combinex 50 mg/ml + 37.5 mg/ml Oral Suspension for Sheep

Active ingredients: Levamisole Hydrochloride, Triclabendazole

Form

Liquid

Species

Sheep

Manufacturer

Elanco GmbH

VMD MA No.

52127/5103

What it's used for

For the treatment and control of parasitic bronchitis, parasitic gastro-enteritis and fascioliasis in sheep. When used at the recommended dose rate, the pr...

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

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Clinical information

Combinex 50 mg/ml + 37.5 mg/ml Oral Suspension for Sheep — SPC Details

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

For the treatment and control of parasitic bronchitis, parasitic gastro-enteritis and
fascioliasis in sheep. When used at the recommended dose rate, the product is
effective against mature and developing immature stages of levamisole-
susceptible Haemonchus, Ostertagia, Trichostrongylus, Cooperia, Nematodirus,
Bunostomum, Chabertia and Oesophagostomum species in the gastro-intestinal
tract, and Dictyocaulus spp in the lungs. It is also effective against all stages of
Triclabendazole susceptible
adult fluke, and so is indicated against both acute and chronic fascioliasis
Revised: June 2025
AN: 00553/2025
Do not mix with other products.
Given as an oral drench. Suitable for use through most types of automatic
drenching gun.
Shake container thoroughly before use and use undiluted product from the
original container.
Unscrew the blue cap from the container and replace it with the white spigot cap
provided. If using an automatic drenching-gun, attach the tube from the
application device to the white spigot cap. After use, remove the white spigot cap
and close the container with the blue cap.

Revised: June 2025
AN: 00553/2025
It can be safely administered to young or pregnant sheep.
To ensure administration of a correct dose, bodyweight should be determined as
accurately as possible; accuracy of the dosing device should be checked.
Recommended dose rate: 7.5 mg levamisole hydrochloride/kg and 10 mg
triclabendazole/kg. This is equivalent to 1 ml of the product per 5 kg bodyweight.
None.
When the product is used at the recommended dose rate and animals are
not overly stressed, side effects are rare. At higher dosages, transient side
effects due to levamisole may occur (i.e. salivation and slight muscle
tremors).
Efficacy of this product against roundworms is reduced if levamisole resistant
strains are present. Efficacy of this product against liver fluke is reduced if
triclabendazole resistant strains are present.

i. Special precautions for use in animals
Assess bodyweight as accurately as possible before calculating the dosage.
Animals must not be treated within a period of 14 days before or after
treatment with organophosphorus compounds.
Clean drenching equipment before and after use.
Intensive use or misuse of anthelmintics can give rise to resistance. To
reduce this risk, dosing programmes should be discussed with your Veterinary
Adviser.
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.
•
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 TeladorsagiaCooperia and
Trichostrongylus
the EU. There are reports of resistance in Haemonchus in sheep outside the
EU. Resistance to triclabendazole has been reported in Fasciola species in
small ruminants in a number of countries including ones in the EU. Therefore

Revised: June 2025
AN: 00553/2025
the use of this product should be based on local (regional, farm)
epidemiological information about susceptibility of nematodes and
trematodes and recommendations on how to limit further selection for
resistance to anthelmintics.
ii. Special precautions to be taken by the person administering the
veterinary medicinal product to animals
When using, do not eat, drink or smoke.
Wash splashes from eyes and skin immediately.
Take off immediately any contaminated clothing.
Wash hands and exposed skin before meals and after work.
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 the product,
or sore mouth/throat or fever occurs shortly afterwards, then medical advice
should be sought immediately.
None known.
Do not store above
25°C. Protect from light.
Protect from freezing.
Following withdrawal of the first dose, use the product within 1 year.
Levamisole hydrochloride 3.75
Excipient(s)
Methyl hydroxybenzoate 0.095 antimicrobial preservative
Propyl hydroxybenzoate 0.035 antimicrobial preservative
Benzoic Acid 0.10 Antioxidant
Sodium metabisulphite 0.25 Antioxidant
Disodium edetate 0.13 Antioxidant
In an aqueous suspension
For a 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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