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POM-V Prescription Required

Pigfen 40 mg/g Premix for Medicated Feeding Stuff for Pigs

Active ingredient: Fenbendazole

Form

Premix

Species

Pigs

Manufacturer

Huvepharma NV

VMD MA No.

30282/3017

What it's used for

A broad spectrum anthelmintic for the treatment of pigs infected with mature and immature forms of nematodes of the gastro-intestinal and respiratory tract...

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 Fenbendazole

  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

Pigfen 40 mg/g Premix for Medicated Feeding Stuff for Pigs — SPC Details

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

A broad spectrum anthelmintic for the treatment of pigs infected with mature
and immature forms of nematodes of the gastro-intestinal and respiratory
tracts:
Hyostrongylus rubidus (Red Stomach worm)
Oesophagostomum sp. (Nodular worms)
Ascaris suum (large roundworm)
Trichuris suis (Whipworm)
Also effective in the contol of (Lungworm).
An ovicidal effect on nematode eggs.

Revised: October 2025
AN: 01766/2025
The veterinary medicinal product is suitable for herd medication of pigs. Administer at
a dose rate of 5 mg fenbendazole per kg bodyweight.
May be administered to pigs either as a single dose of 5 mg/kg (migrating larval,
intestinal larval and adult stages) or by divided dose of 0.72 mg/kg over 7 days
(intestinal larval and adult stages) or 0.36 mg/kg over 14 days (intestinal larval and
adult stages).
Single dose treatment
Use the following formula to calculate how much veterinary medicinal product to add
per tonne of feed:
Kg = Bodyweight (kg)
veterinary medicinal product per tonne (Daily feed intake (kg) x 8)
7 day treatment
The standard dose rate can be divided and administered in feed over 7 days. Use the
following formula to calculate how much veterinary medicinal product to add per
tonne of feed:
Kg = Bodyweight (kg)
veterinary medicinal product per tonne (Daily feed intake (kg) x 56)
14 day treatment
The standard dose rate can be divided and administered in feed over 14 days. Use
the following formula to calculate how much veterinary medicinal product to add per
tonne of feed:
Kg = Bodyweight (kg)
veterinary medicinal product per tonne (Daily feed intake (kg) x 112)
To ensure a correct dosage, body weight should be determined as accurately as
possible. If animals are to be treated collectively rather than individually, they should
be grouped according to their bodyweight and dosed accordingly, in order to avoid
under- or overdosing.
The intake of medicated feed depends on the clinical condition of the animals. In
order to obtain the correct dosage, the concentration of fenbendazole may need to
be adjusted accordingly.
For incorporation into dry feed at the registered mill.
A manufacturer who is approved to incorporate veterinary medicinal products, or
premixtures containing such veterinary medicinal products, directly at any
concentration, must be responsible for mixing when incorporation is less than 2 kg
per tonne for final feed
To ensure adequate distribution of the veterinary medicinal product in the final feed it
is recommended to premix the veterinary medicinal product at a ratio of 1:10 with
feed ingredients before blending into the final feed.
If the premix is used for supplementation of pelleted feed, the pelleting temperature
should not exceed 85 °C.
Not to be mixed in liquid feed.
Do not use in cases of hypersensitivity to the active substance, to other
benzimidazoles or to any of the excipients.
None known.
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 its local representative or the national
competent authority via the national reporting system. See also the package leaflet
for respective contact details.
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:
•
extended period of time.
•
misadministration of the veterinary medicinal 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.
The uptake of medication by animals can be altered as a consequence of illness. In
case of insufficient uptake of feed, animals should be treated parenterally.

Special precautions for safe use in the target species
None.
Special precautions to be taken by the person administering the veterinary medicinal
product to animals.
Embryotoxic effects cannot be excluded. Pregnant women must take extra
precautions when handling this veterinary medicinal product.
This veterinary medicinal product may be toxic to humans after ingestion.
Accidental ingestion of the veterinary medicinal product should be avoided.
In case of accidental ingestion, rinse mouth with plenty of clean water and seek
medical advice immediately and show the package leaflet or the label to the
physician.
This veterinary medicinal product may cause eye irritation and skin sensitisation.
Avoid contact with skin and/or eyes.
Personal protective equipment consisting of goggles, impervious gloves and a
disposable half-mask respirator conforming to European Standard EN149 or a non-
disposable respirator to European Standard EN 140 with a filter to EN 143 should be
worn when handling the veterinary medicinal product.
In case of skin and/or eye contact, immediately rinse with plenty of water.
Wash hands after use.
Special precautions for the protection of the environment
The veterinary medicinal product should not be allowed to enter surface waters as it
has harmful effects on aquatic organisms.
Exacerbation of paracetamol hepatotoxicity by fenbendazole cannot be excluded.
This veterinary medicinal product does not require any special storage conditions.
Meat and offal: 4 days.
4.

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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