Benazecare Flavour 20 mg Tablets for Dogs
Active ingredient: Benazepril Hydrochloride
Form
Tablet
Species
Manufacturer
Ecuphar NV
VMD MA No.
32742/4037
What it's used for
Dogs: Treatment of congestive heart failure. Cats: Reduction of proteinuria associated with chronic kidney disease.
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Paying less for Benazepril Hydrochloride
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Benazecare Flavour 20 mg Tablets for Dogs — SPC Details
Source: VMD Summary of Product Characteristics (SPC). Last updated 27 Mar 2026.
Treatment of congestive heart failure.
Cats:
Reduction of proteinuria associated with chronic kidney disease.
food. The duration of treatment is unlimited.
The veterinary medicinal product tablets should be administered orally at a minimum
dose of 0.25 mg (range 0.25 - 0.5) benazepril hydrochloride/kg body weight once
daily, according to the following table:
BENAZECARE FLAVOUR 20 mg
Weight of dog
(kg)
Standard
Dose
Double Dose> 20 – 40
> 40 – 80
0.5 tablet
1 tablet
1 tablet
2 tablets
The dose may be doubled, still administered once daily, to a minimum dose of
0.5 mg/kg (range 0.5 - 1.0), if judged clinically necessary and advised by the
veterinary surgeon.
AN: 02966/2024 & 02968/2024
excipients.
Do not use in cases of hypotension, hypovolaemia, hyponatraemia or acute renal
failure.
Do not use in cases of cardiac output failure due to aortic or pulmonary stenosis.
Do not use during pregnancy or lactation (section 3.7).
Undetermined frequency
(cannot be estimated from the
available data):
Vomiting
Incoordination
Fatigue
Elevated creatinine
1
Transient
In dogs with chronic kidney disease, at the start of therapy. A moderate increase in
plasma creatinine concentrations following the administration of ACE inhibitors is
compatible with the reduction in glomerular hypertension induced by these agents
and is therefore not necessarily a reason to stop therapy in the absence of other
signs.
In double-blind clinical trials in dogs with congestive heart failure, benazepril
hydrochloride was well tolerated with an incidence of adverse reactions lower than
observed in placebo-treated dogs.
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 its local representative or the national
competent authority via the national reporting system. See the package leaflet for
respective contact details.
AN: 02966/2024 & 02968/2024
AN: 02966/2024 & 02968/2024
Special precautions for safe use in the target species:
No evidence of renal toxicity of the veterinary medicinal product has been observed
in dogs during clinical trials, however, as is routine in cases of chronic kidney
disease, it is recommended to monitor plasma creatinine, urea and erythrocyte
counts during therapy.
Special precautions to be taken by the person administering the veterinary medicinal
product to animals
Wash hands after use.
In case of accidental ingestion, seek medical advice immediately and show the
package leaflet or the label to the physician.
Pregnant women should take special care to avoid accidental oral exposure because
angiotensin converting enzyme (ACE) inhibitors have been found to affect the unborn
child during pregnancy in humans.
Special precautions for the protection of the environment:
Not applicable.
combination with digoxin, diuretics, pimobendan and anti-arrhythmic veterinary
medicinal products without demonstrable adverse interactions.
In humans, the combination of ACE inhibitors and Non-Steroidal Anti-Inflammatory
Drugs (NSAIDs) can lead to reduced anti-hypertensive efficacy or impaired renal
function. The combination of benazepril hydrochloride and other anti-hypertensive
agents (e.g. calcium channel blockers, or diuretics), anaesthetics or
sedatives may lead to additive hypotensive effects. Therefore, concurrent use of
NSAIDs or other medications with a hypotensive effect should be considered with
care. Renal function and signs of hypotension (lethargy, weakness etc.) should be
monitored closely and treated as necessary.
Interactions with potassium-preserving diuretics like spironolactone, triamterene or
amiloride cannot be ruled out. It is recommended to monitor plasma potassium levels
when using benazepril hydrochloride
diuretic because of the risk of hyperkalaemia.
Store in a dry place.
Divided tablets should be stored in the blister pack. The blister pack should be
inserted back into the cardboard box.
4.
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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Related Conditions
Other Products Containing Benazepril Hydrochloride
These products share the same active ingredient and may be suitable alternatives. Always consult your vet.
Arixil Vet 20 mg Film-coated Tablet for Dogs
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Banacep Vet 20 mg Film-coated Tablet for Dogs
POM-VLaboratorios Calier, S.A.
Banacep Vet 5 mg Film-coated Tablet for Dogs and Cats Benazepril Hydrochloride
POM-VLaboratorios Calier, S.A.
Banacep Vet 5 mg Film-coated Tablet for Dogs and Cats Benazepril Hydrochloride
POM-VLaboratorios Calier, S.A.
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