Noroclav 500 mg Palatable Tablets for Dogs
Active ingredients: Amoxicillin, Clavulanic Acid
Form
Tablet
Species
Manufacturer
Norbrook Laboratories Limited
VMD MA No.
02000/5013
What it's used for
•Staphylococci or Escherichia coli. •Staphylococci. • It is recommended to carry out suitable tests for sensitivity testing when initiating the treatment....
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Noroclav 500 mg Palatable Tablets for Dogs — SPC Details
Source: VMD Summary of Product Characteristics (SPC). Last updated 27 Mar 2026.
•Staphylococci.
•
It is recommended to carry out suitable tests for sensitivity testing when initiating the
treatment. The treatment should only proceed if sensitivity is proven to the combination.
to avoid underdosing.
Administration is via the oral route. The dosage rate is 12.5 mg combined actives/kg
bodyweight twice daily. The tablets may be crushed and added to a little food.
The following table is intended as a guide to dispensing the product at the standard dose
rate of 12.5 mg/kg twice daily.
Bodyweight (kg)Number of tablets (500 mg) per dose twice daily20 kg ½40 kg 160 kg 1½80 kg 2
AN: 01996/2024 and 01998/2024
Duration of therapy:
Routine cases involving all indications: The majority of cases respond to between 5 and 7
days therapy.
Chronic or refractory cases: In these cases where there is considerable tissue damage, a
longer course of therapy may be required in that it allows sufficient time for damaged
tissue to repair.
Do not use in rabbits, guinea pigs, hamsters or gerbils.
Do not use in animals with serious dysfunction of the kidneys accompanied by anuria and
oliguria.
Do not use where resistance to this combination is known to occur.
Caution is advised in the use in small herbivores other than those listed above.
Do not administer to horses and ruminating animals.
(<1 animal / 10,000 animals treated,
including isolated reports):
Diarrhoea, Vomiting
Allergic reactions (e.g. skin reaction,
anaphylaxis)
Hypersensitivity
1
In these cases, treatment should be withdrawn.
Unrelated to dose.
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 the national competent authority via the
national reporting system. See the package leaflet for respective contact details.
Special precautions for safe use in the target species:
Inappropriate use of the product may increase the prevalence of bacteria resistant to
amoxicillin/clavulanic acid.
In animals with hepatic and renal failure, the dosing regimen should be carefully evaluated.
Use of the product should be based on susceptibility testing and take into account official
and local antimicrobial policies. Narrow spectrum antibacterial therapy should be used for
first line treatment where susceptibility testing suggests likely efficacy of this approach.
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 a skin rash, you should seek medical
advice and show the doctor this warning. Swelling of the face, lips or eyes or difficulty with
breathing are more serious symptoms and require urgent medical attention.
Wash hands after use.
AN: 01996/2024 and 01998/2024
Special precautions for the protection of the environment:
Not applicable.
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.
Store in a dry place.
Divided tablets should be stored in the blister pack.
AN: 01996/2024 and 01998/2024
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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