Noroclav Injection for Cattle, Dogs and Cats
Active ingredients: Amoxicillin, Clavulanic Acid
Form
Injection
Species
Manufacturer
Norbrook Laboratories Limited
VMD MA No.
02000/5021
What it's used for
Klebsiella spp., Proteus spp., Pasteurellae spp,. Fusobacterium necrophorum Bacteroides (including beta-lactamase producing strains), Haemophilus spp, Mora...
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Ask your vet for a written prescription
They must provide one on request. Under the CMA Order the fee is capped at £21 from 2027.
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2
Fill it at a registered online retailer
The CMA found online pharmacies 50–60% cheaper than practice dispensing on common medicines — typically £200–£300 a year.
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Prescription required
Your vet must provide a written prescription on request. You can then purchase from any licensed online retailer.
Noroclav Injection for Cattle, Dogs and Cats — SPC Details
Source: VMD Summary of Product Characteristics (SPC). Last updated 27 Mar 2026.
Bacteroides (including beta-lactamase producing strains), Haemophilus spp,
Moraxella spp and Actinobacillus lignieresi.
AN: 01218/2025, 01219/2025, 01232/2025 & 01234/2025
(b)
diseases including:
Cattle:
Respiratory infections
Soft tissue infections (e.g. joint/navel ill, abscesses etc.)
Metritis
Mastitis.
Dogs and cats:
Respiratory tract infections Urinary tract infections
Skin and soft tissue infections (e.g. abscesses, pyoderma, anal sacculitis and
gingivitis.)
massage the injection site. This veterinary medicinal product does not contain
an antimicrobial preservative. Use a completely dry sterile needle and syringe.
Swab the septum before removing each dose.
Care should be taken to avoid contaminating the remaining contents of a vial
with water. Clavulanic acid is moisture sensitive. It is very important therefore,
that a completely dry needle and syringe is used when extracting suspension
for injection in order to avoid contaminating the remaining contents of the vial
with drops of water. Contamination will result in obvious beads of dark, brown
discolouration corresponding to the introduced water droplets. Material
affected in this way should not be used as it may have significantly reduced
potency.
advised in its use in other very small herbivores.
Very rare
(<1 animal / 10,000 animals
treated, including isolated
reports):
Immediate pain upon injection, Injection site
reaction
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 immediate
packaging for respective contact details.
other beta-lactam antibiotics. Use of the veterinary medicinal product should
be carefully considered when susceptibility testing has shown resistance to
beta-lactam antibiotics because its effectiveness may be reduced.
Special precautions for safe use in the target species:
Do not use in cases of hypersensitivity to penicillin or other substances of the
beta-lactam group.
Use of the product should be based on identification and susceptibility testing
of the target pathogen(s). If this is not possible, therapy should be based on
epidemiological information and knowledge of susceptibility of the target
pathogens at farm level, or at local/regional level.
Use of the product should be in accordance with official, national and regional
antimicrobial policies.
An antibiotic with a lower risk of antimicrobial resistance selection (lower
AMEG category) should be used for first line treatment where susceptibility
testing suggests the likely efficacy of this approach.
Narrow spectrum antibiotic therapy with a lower risk of antimicrobial
resistance selection should be used for first line treatment where susceptibility
testing suggests the likely efficacy of this approach.
AN: 01218/2025, 01219/2025, 01232/2025 & 01234/2025
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 veterinary medicinal product if you know you are
sensitised, or if you have been advised not to work with such preparations.
Handle this veterinary medicinal 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 package leaflet or the label to the
physician. Swelling of the face, lips or eyes or difficulty with breathing are
more serious symptoms and require urgent medical attention.
Wash hands after use.
Special precautions for the protection of the environment:
Not applicable.
None known.
Meat and offal: 42 days
Milk: 80 hours
Animals must not be slaughtered for human consumption during treatment.
Milk for human consumption must not be taken during treatment.
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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