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Animec 10 mg/ml Solution for Injection for Cattle, Pigs and Sheep

Active ingredient: Ivermectin

Form

Injection

Species

Cattle Pigs Sheep

Manufacturer

Chanelle Pharmaceuticals Manufacturing Ltd

VMD MA No.

08749/3141

What it's used for

Treatment of infections with the following parasites in beef and non-lactating dairy cattle, pigs and sheep: Cattle: Gastro-intestinal roundworms (adult an...

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

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Clinical information

Animec 10 mg/ml Solution for Injection for Cattle, Pigs and Sheep — SPC Details

Source: VMD Summary of Product Characteristics (SPC). Last updated 26 Mar 2026.

Treatment of infections with the following parasites in beef and non-lactating dairy cattle,
pigs and sheep:
Cattle:
Gastro-intestinal roundworms (adult and fourth stage larvae):
Ostertagia spp. (including inhibited O.ostertagi)
Haemonchus placei
Trichostrongylus axei
Trichostrongylus colubriformis
Cooperia spp.
Oesophagostomum radiatum
Nematodirus helvetianus (adult)
N. spathiger
Lungworms
Dictyocaulus viviparus.
Warbles:
Hypoderma bovis
H. lineatum.
Mange mites:
Psoroptes bovis
Sarcoptes scabiei var. bovis.

Amended pages: November 2025
AN: 01686/2025
Sucking lice:
Linognathus vituli
Haematopinus eurysternus
The use of the product in cattle should take into account geographical differences in the
occurrence patterns of parasites.
Pigs:
Gastrointestinal roundworms: (adult and fourth stage larvae):
Ascaris suum
Hyostrongylus rubidus
Oesophagostomum spp.
Strongyloides ransomi
Lungworms:
Metastrongylus spp. (adult)
Lice:
Haematopinus suis
Mange mites:
Sarcoptes scabiei var. suis
Sheep:
Gastrointestinal roundworms (adult and fourth-stage larvae):
Teladorsagia circumcincta including inhibited larvae
T. trifurcata
Haemonchus contortus including inhibited larvae
Trichostrongylus axei (adults)
T. colubriformis and T. vitrinus (adults)
Cooperia curticei
Oesophagostomum columbianum
O. venulosum (adults)
Nematodirus filicollis
Chabertia ovina
Trichuris ovis (adults)
Lungworms:
Dictyocaulus filaria (adult and fourth-stage larvae)
Protostrongylus rufescens (adults)
Nasal bots (all larval stages) :
Oestrus ovis.
Mange mites:
Psoroptes ovis
For single administration only by subcutaneous injection. Each ml contains 10 mg of
ivermectin sufficient to treat 50 kg of bodyweight of cattle and sheep, and 33 kg of
bodyweight of pigs. Replace with a fresh sterile needle after every 10 to 12 animals.
Massage the injection site after administration of the product. Injection of wet or dirty
animals is not recommended.
Underdosing could result in ineffective use and may favour resistance development.
To ensure a correct dosage, body weight should be determined as accurately as possible.
If animals are to be treated collectively, reasonably homogeneous groups should be set
up, and all animals of a group should be dosed at the rate corresponding to the heaviest
one.
Accuracy of the dosing device should be thoroughly checked.
Cattle:
The product should be given only by subcutaneous injection at the recommended dosage
level of 200 µg ivermectin per kg bodyweight under the loose skin in front of, or behind, the
shoulder in cattle. This is equivalent to 1 ml per 50 kg bodyweight.
The volume administered per injection site should not exceed 10 ml.
Pigs:
In pigs, the recommended dosage level is 300 µg ivermectin per kg bodyweight. This is
equivalent to 1 ml per 33 kg bodyweight. The recommended route of administration is by
subcutaneous injection into the neck. The volume administered per injection site should
not exceed 5ml.
Young Pigs:
In young pigs, especially those below 16 kg for which less that 0.5 ml of the product is
indicated, dosing accurately is important. The use of a syringe that can accurately deliver
as little as 0.1 ml is recommended.

Amended pages: November 2025
AN: 01686/2025
Sheep
The recommended dose is 200 µg ivermectin per kg bodyweight (corresponding to 1 ml of
the product per 50 kg bw) by subcutaneous injection over the neck.
The volume administered per injection site should not exceed 1ml.
For the treatment and control of sheep scab (Psoroptes ovis), two injections with a seven-
day interval are required to treat clinical signs of scab and to eliminate mites.
In young lambs weighing less than 25 kg give 0.1 ml of the product per 5 kg. The use of a
syringe that can deliver as little as 0.1 ml is recommended.
This product does not contain any antimicrobial preservative. Swab septum before
removing each dose.
When using the 200, 250 or 500ml pack sizes, use only automatic syringe equipment. For
the 50ml pack size, 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 administer by the intravenous or intramuscular route.
Do not use in cases of hypersensitivity to the active substance or to any of excipients.
Do not use in dogs or cats as severe adverse reactions may occur (see also section 4.5).

Amended pages: November 2025
AN: 01686/2025
Cattle
Transitory discomfort has been observed in some cattle. A low incidence of soft tissue
swelling at the injection site has been observed. These reactions have disappeared
without treatment.
Pigs
Mild and transient pain reactions may be seen in some pigs.
All these reactions disappeared without treatment.

Amended pages: November 2025
AN: 01686/2025
Sheep
Immediately following subcutaneous injection, activity suggesting pain, sometimes intense
but usually transient, has been observed in some sheep.
In sheep treatment of psoroptic mange (sheep scab) with one injection is not
recommended because, although a clinical improvement may be seen, elimination of all
mites may not occur.
Sheep scab (Psoroptes ovis) is an extremely contagious external parasite of sheep. To
ensure complete control great care must be taken to avoid re–infestation, as mites may be
viable for up to 15 days off the sheep. It is important that all sheep which have been in
contact with infected sheep are treated. Contact between treated, infected and untreated
flocks must be avoided until at least seven days after treatment.
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 infestation based on its epidemiological features, for each herd or flock.
Repeated use for an extended period, particularly when using the same class of
substances, increases the risk of resistance development. Within a herd or flock,
maintenance of susceptible refugia is essential to reduce that risk. Systematically applied
interval-based treatment and treatment of a whole herd or 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 herd/flock should be sought
from the responsible veterinarian.
Resistance to ivermectin has been reported in in
cattle. in cattle outside the
EU.
In sheep, resistance to ivermectin is widespread in ,
Trichostrongylus spp.,
species.
Multiple resistance was reported in to benzimidazoles,
macrocyclic lactones and levamisole and in
benzimidazoles.
Multiple resistance to macrocyclic lactones has also been reported in scab
mites in sheep and in cattle.
The use of this product should take into account local information about susceptibility of
the target parasites, where available. It is recommended to further investigate cases of
suspected resistance, using an appropriate diagnostic method (e.g. Faecal Egg Count
Reduction Test). Confirmed resistance should be reported to the marketing authorisation
holder or to the competent authorities.

Amended pages: November 2025
AN: 01686/2025

Special precautions for use in animals
In cattle, to avoid secondary reactions due to the death of Hypoderma larvae in the
oesophagus or in the spine it is recommended to administer the product at the end of
warble fly activity and before the larvae reach their resting sites. Consult your veterinarian
on the correct timing of treatment.
Avermectins may not be well tolerated in non-target species. Cases of intolerance with
fatal results are reported in dogs – especially Collies, Old English Sheepdogs and related
breeds and crosses, and also in turtles/tortoises. In addition, care should be taken to avoid
ingestion of spilled product or access to used containers by these other species.
Since ivermectin is highly bound to plasma proteins, special care should be taken in cases
of sick animals or in nutritional conditions associated with low plasma protein levels.
Special precautions to be taken by the person administering the veterinary medicinal
product to animals
'This product may cause eye and skin irritation. Avoid contact with skin or eyes. In case
of skin or eye contact, wash exposed area with plenty of clean water. If symptoms persist,
seek medical advice.
Take care to avoid accidental self-injection: the product may cause local irritation and/or
pain at the site of injection. In case of accidental self-injection, seek immediate medical
advice and show the information leaflet or the label to the physician.
Do not eat or smoke while handling the product.
Wash hands after use.
Other precautions
The product is very toxic to aquatic organisms and dung insects.
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/flock health, as advised by a veterinarian.
Treated cattle should not have direct access to ponds, streams or ditches for 14 days after
treatment.
Do not combine with vaccination against lungworm. If vaccinated animals are to be
treated, treatment should not be carried out within a period of 28 days before or after
vaccination.
This veterinary medicinal product does not require any special storage precautions.
Cattle
Meat and offal: 49 days.
Do not use in lactating cows producing milk for human consumption. Do not use in cattle
producing milk for human consumption or in dairy cows within 60 days prior to calving.
Pigs
Meat and offal: 28 days.
Sheep
Meat and offal: 25 days
Do not use in lactating sheep producing milk for human consumption.
Do not use in sheep within 60 days of lambing where milk is to be used for human
consumption

Amended pages: November 2025
AN: 01686/2025
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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