Elanco Milbemycin - Praziquantel 2.5 mg/25 mg Chewable Tablets for Small Dogs and Puppies
Active ingredients: Milbemycin Oxime (A3 and A4), Praziquantel
Form
Chewable
Species
Manufacturer
Elanco Europe Ltd
VMD MA No.
00879/5006
What it's used for
In dogs: treatment of mixed infections by adult cestodes and nematodes of the following species susceptible to praziquantel and milbemycin oxime: - Cestode...
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Elanco Milbemycin - Praziquantel 2.5 mg/25 mg Chewable Tablets for Small Dogs and Puppies — SPC Details
Source: VMD Summary of Product Characteristics (SPC). Last updated 18 Mar 2026.
following species susceptible to praziquantel and milbemycin oxime:
- Cestodes:
Dipylidium caninum
Taenia spp.
Echinococcus spp.
Mesocestoides spp.
- Nematodes:
Ancylostoma caninum
Toxocara canis
Toxascaris leonina
Trichuris vulpis
Issued December 2022
AN: 00874/2022
Crenosoma vulpis
Angiostrongylus vasorum
and adult parasite stages) (see specific treatment and prevention disease schedules
under section 4.9 “Amounts to be administered and administration route”)
Thelazia callipaeda
administered and administration route”)
The product can also be used in the prevention of heartworm disease (Dirofilaria
immitis) if concomitant treatment against cestodes is indicated.
praziquantel per kg are given once orally. The product should be administered with or
after some food.
Depending on the bodyweight of the dog, the practical dosing is as follows:
1 – 5 kg 1 tablet
To ensure a correct dosage, body weight should be determined as accurately as possible to
avoid under dosing.
In cases when heartworm disease prevention is used and at the same time treatment against
tapeworm is required, the product can replace the monovalent product for the prevention of
heartworm disease.
For treatment of Angiostrongylus vasorum infections, milbemycin oxime should be given four
times at weekly intervals. It is recommended, where concomitant treatment against cestodes
is indicated, to treat once with the product and continue with the monovalent product
containing milbemycin oxime alone, for the remaining three weekly treatments.
In endemic areas administration of the product every four weeks will prevent
angiostrongylosis by reducing immature adult (L5) and adult parasite burden, where
concomitant treatment against cestodes is indicated.
For the treatment of Thelazia callipaeda
seven days apart. Where concomitant treatment against cestodes is indicated, the product
can replace the monovalent product containing milbemycin oxime alone.
Do not use in cases of hypersensitivity to the active substances or to any of the
excipients
See also section 4.5 "Special precautions for use".
neurological signs (such as muscle tremors, ataxia and convulsions) and/or gastrointestinal
signs (such as emesis, drooling, diarrhoea and anorexia) have been observed in dogs after
administration of the veterinary medicinal product.
The frequency of adverse reactions is defined using the following convention:
- very common (more than 1 in 10 animals treated displaying adverse reaction(s))
- common (more than 1 but less than 10 animals in 100 animals treated)
- uncommon (more than 1 but less than 10 animals in 1,000 animals treated)
- rare (more than 1 but less than 10 animals in 10,000 animals treated)
- very rare (less than 1 animal in 10,000 animals treated, including isolated reports).
When infection with the cestode has been confirmed, concomitant treatment
against intermediate hosts, such as fleas and lice, should be discussed with a veterinarian to
prevent re-infection.
The use of the product should follow the implementation of appropriate diagnostic measures
towards mixed infections by nematodes and cestodes with consideration of animal history
and characteristics (e.g. age, health status), environment (e.g. kennelled dogs, hunting
dogs), feeding (e.g. access to raw meat), geographical location and travel. Judgement of the
administration of the product in dogs at risk from mixed re-infections or in specific at risk
situations (such as zoonotic risks), should be made by the veterinarian responsible.
Special precautions for use in animals
Studies with milbemycin oxime indicate that the margin of safety in certain dogs of Collie or
related breeds is less than in other breeds. In these dogs, the recommended dose should be
strictly observed.
The tolerance of the product in young puppies from these breeds has not been investigated.
Clinical signs in Collies are similar to those seen in the general dog population when
overdosed (see section 4.10 “Overdose”).
Treatment of dogs with a high number of circulating microfilariae can sometimes lead to the
appearance of hypersensitivity reactions, such as pale mucous membranes, vomiting,
trembling, laboured breathing or excessive salivation. These reactions are associated with
the release of proteins from dead or dying microfilariae and are not a direct toxic effect of the
product. The use in dogs suffering from microfilaremia is thus not recommended.
In heartworm risk-areas, or in the case it is known that a dog has been travelling to and from
heartworm risk regions, before using the product, a veterinary consultation is advised to
exclude the presence of any concurrent infestation of Dirofilaria immitis. In the case of a
positive diagnosis, adulticidal therapy is indicated before administering the product.
No studies have been performed with severely debilitated dogs or individuals with seriously
compromised kidney or liver function. The product is not recommended for such animals or
only according to a benefit/risk assessment by the responsible veterinarian.
Issued December 2022
AN: 00874/2022
In dogs less than 4 weeks old, tape worm infection is unusual. Treatment of animals less
than 4 weeks old with a combination product may therefore not be necessary.
Parasite resistance to any particular class of anthelmintic may develop following frequent,
repeated use of an anthelmintic of that class
Special precautions to be taken by the person administering the veterinary medicinal
product to animals
Wash hands after use.
People with known hypersensitivity to any of the ingredients should avoid contact with the
veterinary medicinal product. In case of accidental ingestion of the tablets, particularly by a
child, seek medical advice immediately and show the package leaflet or the label to the
physician. Echinococcosis represents a hazard for humans. In case of Echinococcosis,
specific guidelines on the treatment and follow up and on the safeguard of persons have to
be followed. Experts or institutes of parasitology should be consulted.
selamectin was administered during treatment with the product at the recommended dose.
Although not recommended, the concomitant use of the product with a spot on containing
moxidectin and imidacloprid at recommended dose rates following a single application was
well tolerated in one experimental study by beagle dogs at the age 11 months or older.
Transient neurological adverse reactions (poor proprioception, flaccid frontal and hind legs,
incoordination, slight tremors and high stepping gait of the hind limbs only) were observed
after concurrent administration of both products in another study conducted in puppies aged
8-12 weeks. Such signs were however not observed in this study after giving Elanco
Milbemycin - Praziquantel alone.
The safety and efficacy of this combination have not been investigated in field studies.
In the absence of further studies, caution should be taken in the case of concurrent use of
Elanco Milbemycin - Praziquantel and any other macrocyclic lactone. Also, no such studies
have been performed with reproducing animals, Collies, related breeds and their crosses.
Issued December 2022
AN: 00874/2022
Propylene glycol (E 1520) 0.91 mg
Iron oxide, brown (E 172) 0.66 mg
Butylhydroxyanisole (E 320) 0.26 mg
Propyl gallate (E 310) 0.09 mg
For the full list of excipients, see section
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 Milbemycin Oxime (A3 and A4)
These products share the same active ingredient and may be suitable alternatives. Always consult your vet.
Aderexa 12.5 mg/125 mg Chewable Tablets for Dogs Weighing at Least 5 kg
POM-VKRKA, d.d., Novo mesto
Aderexa 2.5 mg/25 mg Chewable Tablets for Small Dogs and Puppies Weighing at Least 0.5 kg
POM-VKRKA, d.d., Novo mesto
Alpramil 12 mg/30 mg Film-coated Tablets for Cats Weighing at Least 3 kg
POM-VAlfasan Nederland B.V.
Alpramil 12 mg/30 mg Film-coated Tablets for Cats Weighing at Least 3 kg
POM-VAlfasan Nederland B.V.
Alpramil 12.5 mg/125 mg Tablets for Dogs Weighing at Least 5 kg
POM-VAlfasan Nederland B.V.
Alpramil 12.5 mg/125 mg Tablets for Dogs Weighing at Least 5 kg
POM-VAlfasan Nederland B.V.
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