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POM-VPS Prescription Required

Zolvix 25 mg/ml Oral Solution for Sheep

Active ingredient: Monepantel

Form

Liquid

Species

Sheep

Manufacturer

Elanco GmbH

VMD MA No.

EU/2/09/101/001-010

What it's used for

ZOLVIX oral solution is a broad spectrum anthelmintic for the treatment of gastro- intestinal nematode infections and associated diseases in sheep includin...

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 Monepantel

  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

Zolvix 25 mg/ml Oral Solution for Sheep — SPC Details

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

ZOLVIX oral solution is a broad spectrum anthelmintic for the treatment of gastro-
intestinal nematode infections and associated diseases in sheep including lambs,
hoggets, breeding rams and ewes.

Issued: August 2023
AN: 01900/2022
Spectrum of activity includes fourth larvae and adults of:Haemonchus contortus*Teladorsagia circumcincta*Teladorsagia trifurcata*Teladorsagia davtiani*Trichostrongylus axei*Trichostrongylus colubriformisTrichostrongylus vitrinusCooperia curticeiCooperia oncophoraNematodirus battusNematodirus filicollisNematodirus spathigerChabertia ovina Oesophagostomum venulosum
*including inhibited larvae
None.
Target species: sheep
None.
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 the national
competent authority via the national reporting system. See also the last
section of the package leaflet for contact details.
Unnecessary use of antiparasitics or use deviating from the instructions given
in the SPC may increase the resistance selection pressure and lead to
reduced efficacy. The decision to use the product should be based on
confirmation of the parasitic species and burden, or of the risk of infection
based on its epidemiological features, for each flock.
Repeated use for an extended period, particularly when using the same class
of substances, increases the risk of resistance development. Within a flock,
maintenance of susceptible refugia is essential to reduce that risk.
Systematically applied interval-based treatment and treatment of a whole flock
should be avoided. Instead, if feasible, only selected individual animals or
subgroups should be treated (targeted selective treatment). This should be
combined with appropriate husbandry and pasture management measures.
Guidance for each specific flock should be sought from the responsible
veterinarian.
Isolated cases of resistance against monepantel have been identified within
the European Union.
The use of this product should take into account local information about
susceptibility of the target parasites, where available.
In order to help delay the development of resistance, users are advised to
check the success of the treatment (e.g. clinical appearance, faecal egg
counts). It is recommended to further investigate cases of suspected
resistance, using an appropriate diagnostic method (e.g. Faecal Egg Count
Reduction Test). Where the results of the tests strongly suggest resistance to

Issued: August 2023
AN: 01900/2022
a particular anthelmintic, an anthelmintic belonging to another
pharmacological class and having a different mode of action should be used.
Confirmed resistance should be reported to the marketing authorisation holder
or to the competent authorities.

i) Special precautions for use in animals
The safety has not been established in sheep weighing less than 10 kg or
under 2 weeks of age.
ii) Special precautions to be taken by the person administering the veterinary
medicinal product to animals
Personal protective equipment consisting of gloves should be worn when
handling the veterinary medicinal product.
In case of accidental spillage onto skin or into eyes, wash immediately with
water. Take off any contaminated clothes. In case of accidental ingestion seek
medical advice immediately and show the package leaflet or the label to the
physician.
Do not eat, drink or smoke whilst handling the veterinary medicinal product.
Wash hands and exposed skin after handling the veterinary medicinal
product.
iii) Special precautions for the protection of the environment:
Not applicable
None known.
This veterinary medicinal product does not require any special storage
conditions.
Meat and offal: 7 days.
Not authorised for use in animals 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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Same active ingredient

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