Closamectin Solution for Injection for Cattle
Active ingredients: Closantel, Ivermectin
Form
Injection
Species
Manufacturer
Norbrook Laboratories Limited
VMD MA No.
02000/3000
What it's used for
Gastrointestinal roundworms Ostertagia ostertagi Haemonchus placei Trichostrongylus colubriformis immature), immature) (adult), phlebotomum (adult and imma...
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Prescription required
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Closamectin Solution for Injection for Cattle — SPC Details
Source: VMD Summary of Product Characteristics (SPC). Last updated 27 Mar 2026.
Ostertagia ostertagi
Haemonchus placei
Trichostrongylus colubriformis
immature),
immature)
(adult),
phlebotomum (adult and immature), Toxocara vitulorum Trichuris spp.
Lungworms
Dictyocaulus viviparus
th
stage larvae)
Liver Fluke (trematodes)
Fasciola hepatica
Treatment of fluke at 12 weeks (mature).
Treatment of fluke from 9 weeks (late immature) >90% efficacy
Eyeworms (adult)
Thelazia spp
Cattle grubs (parasitic stages)
Hypoderma bovis, Hypoderma lineatum
Lice
Linognathus vituli, Haematopinus eurysternus, Solenopotes capillatus
Mange Mites
Psoroptes ovis (syn var bovis), Sarcoptes scabiei var bovis
The veterinary medicinal product may also be used as an aid in the control of the biting
louse , but complete elimination
may not occur.
Persistent activity
When cattle have to graze on pasture contaminated with infective larvae of cattle
nematodes, treatment with the veterinary medicinal product at the recommended dose
rate of 200 µg ivermectin per kg bodyweight and 5 mg closantel per kg bodyweight
controls re-infection with:
Prolonged activity
Dictyocaulus viviparus
Up to 21 days
Ostertagia ostertagi
Up to 21 days
Oesophagostomum radiatum
Up to 21 days
Cooperia spp
Up to 14 days
Trichostrongylus axei
Up to 14 days
Haemonchus placei
Up to 14 days
be administered at any one site with any residual volume administered at another site in
the neck. A sterile 16-gauge, one-inch needle is recommended.
This product does not contain an antimicrobial preservative. Swab septum before
removing each dose. Use a dry sterile needle and syringe. For 250 ml and 500 ml pack
sizes, use of a multiple dose syringe is recommended. To refill the syringe, use of a
draw-off needle is recommended to avoid excessive broaching of the stopper.
Do not exceed 40 broachings per vial. If more than 40 broachings are required, use of a
draw off needle is recommended.
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.
To ensure administration of a correct dose, bodyweight should be determined as
accurately as possible; accuracy of the dosing device should be checked.
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 over-
dosing.
Avermectins may not be well tolerated in all non-target species (cases of intolerance with
fatal outcome are reported in dogs – especially Collies, Old English Sheepdogs and
related breeds or crosses, and also in turtles/tortoises).
Do not use in cases of known hypersensitivity to the active substances or to any of the
excipients.
treated):
Injection site
swelling
Injection site pain
1
Injection site pain is common and will resolve thereafter without treatment. Swelling and
hardness on palpation may be observed up to 40 days following administration.
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 ‘Contact details’ section of the
package leaflet.
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.
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
tests 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
of this product should be based on local epidemiological information about the
susceptibility of the
for resistance to anthelmintics.
Special precautions for safe use in the target species:
Not Applicable.
Special precautions to be taken by the person administering the medical veterinary
product to animals
Do not smoke, eat or drink while handling the product.
Avoid direct contact of the product with the skin. In case of spillage onto the skin rinse
immediately with fresh water.
Wash hands after use.
Take care to avoid self-injection. Inadvertent self-injection may result in local irritation
and/or pain at the injection site.
In case of accidental self-injection, seek medical advice immediately and show the
package leaflet or the label to the physician.
Special precautions for the protection of the environment:
Ivermectin is very toxic to aquatic organisms and dung insects. Treated cattle should not
have direct access to ponds, streams or ditches for 14 days after treatment. Long term
effects on dung insects caused by continuous or repeated use cannot be excluded.
Therefore repeated treatment of animals on a pasture with an ivermectin-containing
product within a season should only be given in the absence of alternative treatments or
approaches to maintain animal/herd health, as advised by a veterinarian.
agonists are increased by ivermectin. Please refer to section 4.2 of the SPC.
Protect from light.
Milk: Not authorised for use in cattle producing milk for human consumption including
during the dry period. Do not use during the last trimester of pregnancy in heifers which
are 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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Related Conditions
Other Products Containing Closantel
These products share the same active ingredient and may be suitable alternatives. Always consult your vet.
Closamectin 5 mg/ml + 200 mg/ml Pour-on Solution for Cattle
POM-VPSNorbrook Laboratories Limited
Closamectin 5 mg/ml + 200 mg/ml Pour-on Solution for Cattle
POM-VPSNorbrook Laboratories Limited
Closamectin 5 mg/ml/125 mg/ml Solution for Injection for Sheep
POM-VPSNorbrook Laboratories Limited
Closamectin Solution for Injection for Cattle
POM-VPSNorbrook Laboratories Limited
Closiver 5 mg/ml + 125 mg/ml Solution for Injection for Sheep
POM-VPSNorbrook Laboratories Limited
Flukiver 50 mg/ml Oral Suspension
POM-VPSElanco GmbH
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