Triclacert Duo 50 mg/ml & 1 mg/ml Oral Suspension for Sheep
Active ingredients: Ivermectin, Triclabendazole
Form
Paste
Species
Manufacturer
Chanelle Pharmaceuticals Manufacturing Ltd
VMD MA No.
08749/5202
What it's used for
Gastrointestinal nematodes (adult and immature): Haemonchus contortus, Teladorsagia (Ostertagia) circumcincta, Trichostrongylus spp, Cooperia spp, Nematodi...
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Prescription required
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Triclacert Duo 50 mg/ml & 1 mg/ml Oral Suspension for Sheep — SPC Details
Source: VMD Summary of Product Characteristics (SPC). Last updated 27 Mar 2026.
Haemonchus contortus, Teladorsagia (Ostertagia) circumcincta, Trichostrongylus
spp, Cooperia spp, Nematodirus spp including N. battus, Strongyloides papillosus,
Oesophagostomum spp, and adult
Inhibited larval stages and benzimidazole resistant strains of Haemonchus contortus
and Teladorsagia (Ostertagia) circumcincta are also controlled.
Liver fluke (mature, immature and early immature stages down to less than 1
week of age):
Fasciola hepatica
Lungworms (adult and immature):
Dictyocaulus filaria
Nasal bots (all stages):
Oestrus ovis
equivalent to 2 ml/10 kg bodyweight.
To ensure a correct dosage, bodyweight should be determined as accurately as
possible. The product is for oral administration using a suitably calibrated dosing
gun. The container should be shaken thoroughly before use. Drenching equipment
should be cleaned before and after use.
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 timing for treatment should be based on epidemiological factors and should be
customised for each individual farm. As with other anthelmintics, veterinary advice
should be sought on appropriate dosing programmes and stock management to
achieve adequate parasite control and reduce the likelihood of resistance
developing.
Dosing Table:
Animal WeightDose of the product20 – 25 kg5 ml26 – 30 kg6 ml31 – 35 kg7 ml36 – 40 kg8 ml41 – 50 kg10 ml51 – 60 kg12 ml61 – 70 kg14 ml71 – 80 kg16 ml81 – 90 kg18 ml91 – 100 kg20 ml
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 the package leaflet for
respective contact details.
of development of resistance and could ultimately result in ineffective therapy:
• Too frequent and repeated use of anthelmintics from the same class,
over an extended period of time.
• Underdosing which may be due to underestimation of bodyweight,
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 ivermectin has been reported in Teladorsagia (Ostertagia)
circumcincta,Haemonchus contortus Trichostrongylus species in sheep, and
increasing resistance to triclabendazole has been reported in Fasciola species in
sheep in a number of countries including in Europe.
Therefore, the use of this product should be based upon local (regional, farm)
epidemiological information about susceptibility of the target parasites and
recommendations on how to limit further selection for resistance to anthelmintics.
Special precautions for safe use in the target species:
Extra-label use in dogs should be avoided as severe adverse reactions may occur. In
common with other avermectins, certain breeds of dogs, such as Collies are
especially sensitive to ivermectin and particular care should be taken to avoid
accidental consumption of the product.
Special precautions to be taken by the person administering the veterinary medicinal
product to animals
• This product may cause hypersensitivity (allergic) reactions. People with
known hypersensitivity to ivermectin, triclabendazole or parabens should
avoid contact with the product.
• This product may cause skin and eye irritation.
• Avoid direct contact with the skin and eyes.
• Protective gloves should be worn when handling the product.
• In case of accidental spillage onto skin or into the eyes wash immediately with
water. Take off any contaminated clothes.
• Do not eat, drink or smoke whilst handling the product.
• Wash hands and any exposed skin before meals and after work.
Special precautions for the protection of the environment:
Long-term effects on dung insects caused by continuous or repeated use cannot be
excluded. The risk to aquatic ecosystems and dung fauna can be reduced by
avoiding too frequent and repeated use of this product and other products of the
same anthelmintic class in cattle, sheep and pigs. Therefore, the repetition of
treatment in a pasture during a season should be performed only in the absence of
alternative treatment and on veterinary advice.
Store in the original container.
Protect from light.
Do not freeze. Protect from frost.
Milk: Not permitted for use in ewes producing milk for human consumption including
during the dry period. Do not use within 1 year prior to the first lambing in ewes
intended to produce milk for human consumption.
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 Ivermectin
These products share the same active ingredient and may be suitable alternatives. Always consult your vet.
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