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POM-V Prescription Required Companion Animal

Amoxibactin 50 mg Tablets for Dogs and Cats

Active ingredient: Amoxicillin

Form

Tablet

Species

Cats Dogs

Manufacturer

Le Vet Beheer B.V.

VMD MA No.

41821/4014

View official SPC (PDF)

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Prescription required

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Clinical information

Amoxibactin 50 mg Tablets for Dogs and Cats — SPC Details

Source: VMD Summary of Product Characteristics (SPC). Last updated 18 Mar 2026.

Treatment of primary and secondary infections of the airways, such as rhinitis caused
by Pasteurella spp. and Streptococcus spp., and bronchopneumonia caused by
Pasteurella spp., Escherichia coli and Gram-positive cocci.
Treatment of primary infections of the urogenital tract, such as pyelonephritis and
infections of the lower urinary tract caused by
Gram-positive cocci, endometritis caused by Escherichia coli, Streptococcus canis
and Proteus spp., and vaginitis as a result of mixed infections.
Treatment of mastitis caused by Gram-positive cocci and Escherichia coli.
Treatment of local skin infections caused by spp.
For oral administration in dogs and cats.
To ensure a correct dosage body weight should be determined as accurately as
possible to avoid underdosing.
Dosage
The recommended dose is 10 mg amoxicillin per kg bodyweight, twice daily for a
minimum of 5 consecutive days. The majority of routine cases respond after between
5 and 7 days of therapy. If no improvement is observed after 5 – 7 days, the
diagnosis should be re-assessed. In chronic or refractory cases, a longer course of
therapy may be required.

Revised: July 2020
AN: 00931/2019Page 4 of 7
The following table is intended as a guide to dispensing the product at the standard
dose rate of 10 mg per kg bodyweight twice daily.
Number of tablets twice daily
Body weight
(kg)
Amoxicillin 50
mg
for dogs and
cats
Amoxicillin 250
mg
for dogs
Amoxicillin 500
mg
for dogs
1 – 1.25 >1.25 – 2.5 >2.5 – 3.75 >3.75 – 5 >5 – 6.25
or
>6.25 – 12.5
or
>12.5 – 18.75 >18.75 - 25
or
>25 – 31.25 >31.25 – 37.5
or
>37.5 - 50
or
>50 – 62.5 >62.5 - 75
= ¼ Tablet = ½ Tablet = ¾ Tablet = 1 Tablet
Tablets can be divided into halves or quarters to ensure accurate dosing. Place the
tablet on a flat surface, with its scored side facing up and the convex (rounded) side
facing the surface.
Halves: press down with your thumbs on both sides of the tablet.
Quarters: press down with your thumb in the middle of the tablet.
Do not use in known cases of hypersensitivity to penicillins or other substances of the
β-lactam
Do not administer to gerbils, guinea pigs, hamsters, rabbits and chinchillas.
Do not use in animals with serious renal dysfunction accompanied by anuria or
oliguria.

Revised: July 2020
AN: 00931/2019Page 2 of 7
Mild gastrointestinal symptoms (diarrhoea and vomiting) may occur very rarely (less
than 1 animal in 10,000 animals treated, including isolated reports) after
administration of the product. Hypersensitivity reactions (allergic skin reactions,
anaphylaxis) may occur very rarely. In these cases, administration should be
discontinued and a symptomatic treatment given.

Revised: July 2020
AN: 00931/2019Page 3 of 7
None

Special precautions for use in animals
In animals with hepatic and renal dysfunction, the dosing regimen should be carefully
evaluated and the use of the product based on a risk/benefit evaluation by the
veterinary surgeon.
Caution is advised in the use in small herbivores other than those which have been
contraindicated in the section 4.3.
Due to the likely variability (time, geographical) in the occurrence of resistance of
bacteria for amoxicillin, bacteriological sampling and susceptibility testing are
recommended. Increased antimicrobial resistance are reported among E. Coli
isolates including multidrug-resistant E. Coli. Special precautions should be taken
when multi-drug resistance are suspected based on susceptibility testing. Whenever
possible, the product should only be used based on susceptibility testing.
Use of the product deviating from the instructions given in the SPC may increase the
prevalence of bacteria resistant to amoxicillin and may decrease the effectiveness of
treatment with other beta lactam antimicrobials or other classes of antimicrobials due
to the potential for cross resistance.
Official, national and regional antimicrobial policies should be taken into account
when product is used.
The tablets are flavoured. In order to avoid any accidental ingestion, store tablets out
of reach of the animals.
Special precautions to be taken by the person administering the veterinary
medicinal product to animals
Penicillins and cephalosporins may cause hypersensitivity (allergy) following
injection, inhalation, ingestion or skin contact. Hypersensitivity to penicillins may lead
to cross reactions to cephalosporins and vice versa. Allergic reactions to these
substances may occasionally be serious.
Do not handle this product if you know you are sensitised, or if you have been
advised not to
work with such preparations.
Handle this product with great care to avoid exposure, taking all recommended
precautions.
If you develop symptoms following exposure, such as skin rash, you should seek
medical advice and show the doctor this warning. Swelling of the face, lips or eyes or
difficulty breathing are more serious symptoms and require urgent medical attention.
Wash hands after handling the tablets.
Chloramphenicol, macrolides, sulfonamides and tetracyclines may inhibit the
antibacterial effect of penicillins because of the rapid onset of bacteriostatic action.
The potential for allergic cross-reactivity with other penicillins should be considered.
Penicillins may increase the effect of aminoglycosides.
Do not store above 30C.
Any unused tablet portion should be returned to the open blister and used within 4
days.
Not applicable.
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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