Tilmicosol 250 mg/ml Solution for Use in Drinking Water/Milk
Active ingredient: Tilmicosin
Form
Solution
Species
Manufacturer
Lavet Pharmaceuticals Ltd
VMD MA No.
32823/4003
What it's used for
Pigs: For the treatment with Mycoplasma hyopneumoniae, Pasteurella multocida, Actinobacillus pleuropneumoniae susceptible to tilmicosin. Chickens: For the...
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Tilmicosol 250 mg/ml Solution for Use in Drinking Water/Milk — SPC Details
Source: VMD Summary of Product Characteristics (SPC). Last updated 26 Mar 2026.
with Mycoplasma hyopneumoniae, Pasteurella multocida, Actinobacillus
pleuropneumoniae susceptible to tilmicosin.
Chickens: For the treatment
associated with Mycoplasma gallisepticum and M. synoviae susceptible to tilmicosin.
Turkeys: For the treatment
associated with Mycoplasma gallisepticum and M. synoviae susceptible to tilmicosin.
Calves: For the treatment and
Mannheimia haemolytica, Pasteurella multocida, Mycoplasma bovis, M. dispar susceptible
to tilmicosin
Revised: November 2023
AN: 01156/2023 & 01157/2023Page 2 of 7
The presence of the disease in the group/flock must be established before the product is
used.
The product must be diluted in drinking water (pigs, chickens, turkeys) or milk replacer
(calves) before administration.
Calves: 12.5 mg tilmicosin/kg body weight (i.e.1 ml of product per 20 kg body weight),
twice daily, for 3-5 consecutive days.
Pigs: 15-20 mg tilmicosin/kg body weight/day (i.e. 6-8 ml of product per 100 kg of body
weight per day), for 5 consecutive days, which may be achieved by the inclusion of 150-
200 mg of tilmicosin per litre (60-80 ml of product per 100 litres based on a water
consumption of 10 % of bodyweight).
Chickens: 15-20 mg tilmicosin/kg body weight/day (i.e. 6-8 ml of product per 100 kg of
body weight per day), for 3 consecutive days, which may achieved by the inclusion of 75-
100 mg of tilmicosin per litre (30-40 ml of product per 100 litres
consumption of 20 % of bodyweight).
Turkeys: 10-27 mg tilmicosin/kg body weight/day (i.e. 4-11 ml of product per 100 kg of
body weight per day), for 3 consecutive days, which may achieved by the inclusion of 143-
386 mg of tilmicosin per litre (57-154 ml of product per 100 litres
consumption of 7 % of bodyweight).
If signs of disease do not significantly improve within 3-5 days, the diagnosis should be re-
evaluated and treatment changed.
The exact concentration of the veterinary medicinal product required can be calculated
according to the following formula:
ml product per litre drinking water per day = [ml product per kg bodyweight per day x
average bodyweight (kg)] / average daily water intake (litre).
Bodyweight should be determined as accurately as possible to avoid under-dosing. The
required dose should be measured using suitably calibrated measuring equipment. Only
sufficient medicated drinking water should be prepared to cover the daily requirements.
Revised: November 2023
AN: 01156/2023 & 01157/2023Page 4 of 7
The medicated water should be the only source of drinking water for the animals for the
entire duration of the treatment period. Water intake should be monitored at frequent
intervals during medication. After the end of the medication period, the water supply
system should be cleaned appropriately to avoid intake of sub-therapeutic amounts of the
active substance.
Medicated drinking water should be prepared fresh every 24 hours. Medicated milk
replacer should be prepared fresh every 6 hours.
The medicinal product should be diluted with water or milk replacer prior to its use. When
preparing a stock solution, the maximum concentration should not exceed 200 ml of
product/litre. The lowest concentrations of the product at which stability can be assured
are 0.3 ml product/litre drinking water and 0.8 ml product/litre milk replacer.
The uptake of medicated drinking water/milk replacer depends on the clinical condition of
the animals. In order to obtain the correct dosage, the concentration of the product should
be adjusted accordingly.
Do not use in case of hypersensitivity to tilmicosin or to any of the excipients.
Do not administer to ruminating animals with active rumen function.
decrease in water intake has been observed.
Pigs, chickens and turkeys: Water consumption should be monitored in order to guarantee
adequate dosing. In case water consumption does not match quantities for which
recommended concentrations were calculated, the concentration of product has to be
adapted in a way that the recommend dosage will be taken up by the animals or different
medication should be considered.
The uptake of medication by animals can be altered as a consequence of illness. In case
of insufficient uptake of water or milk replacer, animals should be treated parenterally
using an appropriate injectable product.
Repeated use of the product should be avoided by improving management practices and
thorough cleansing and disinfection.
Special precautions for use in animals
For oral use only. Contains disodium edetate; do not inject.
Inappropriate use of the product may increase the prevalence of bacteria resistant to
tilmicosin and may decrease the effectiveness of treatment with tilmicosin-related
substances. The use of the product should be based on susceptibility tests.
Official, national and regional antimicrobial policies should be taken into account when the
product is used.
Special precautions to be taken by the person administering the veterinary medicinal
product to animals
Tilmicosin may induce irritation. Macrolides, such as tilmicosin, may also cause
hypersensitivity (allergy) following injection, inhalation, ingestion or contact with skin or
eye. Hypersensitivity to tilmicosin may lead to cross reactions to other macrolides and vice
versa. Allergic reactions to these substances may occasionally be serious and therefore
direct contact should be avoided.
To avoid exposure during preparation of the medicated drinking water, wear overalls,
safety glasses, and impervious gloves. Do not eat, drink or smoke when handling this
product. Wash hands after use.
In the case of accidental ingestion, wash out mouth immediately with water and seek
medical advice. In the event of accidental skin contact, wash thoroughly with soap and
water. In case of accidental eye contact, flush the eyes with plenty of clean, running water.
Do not handle the product if you are allergic to ingredients in the product.
If you develop symptoms following exposure, such as skin rash, you should seek medical
advice and show the physician this warning. Swelling of the face, lips and eyes or difficulty
in breathing are more serious symptoms and require urgent medical attention.
Revised: November 2023
AN: 01156/2023 & 01157/2023Page 3 of 7
Do not use simultaneously with bacteriostatic antimicrobials.
freeze.
Meat and offal: 14 days
Chicken
Meat and offal: 12 days
Not authorised for use in birds producing eggs for human consumption. Do not use within
14 days of the start of the laying period.
Turkeys
Meat and offal: 19 days
Revised: November 2023
AN: 01156/2023 & 01157/2023Page 5 of 7
Calves
Meat and offal: 42 days
Not authorised for use in animals producing milk for human consumption.
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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Other Products Containing Tilmicosin
These products share the same active ingredient and may be suitable alternatives. Always consult your vet.
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POM-VNimrod Nederland B.V.
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Milbotyl 300 mg/ml Solution for Injection for Cattle and Sheep
POM-VChanelle Pharmaceuticals Manufacturing Ltd
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