Ridaworm Wormer Granules 888 mg for Adult Dogs (Fenbendazole)

Fenbendazole

Last verified

Veterinary medicinal product: granules. Distribution category: AVM-GSL (Veterinary Medicines Regulations 2013, Schedule 3). Active substance: Fenbendazole.1

In short: questions and answers

Does Ridaworm Wormer Granules 888 mg for Adult Dogs (Fenbendazole) need a prescription?
Over the counter. As stated in the registration decision.1
Which animals is Ridaworm Wormer Granules 888 mg for Adult Dogs (Fenbendazole) for?
Dogs.1
What is the active substance in Ridaworm Wormer Granules 888 mg for Adult Dogs (Fenbendazole)?
Fenbendazole. ATCvet code: QP52AC13.13
What is the withdrawal period of Ridaworm Wormer Granules 888 mg for Adult Dogs (Fenbendazole) according to the leaflet?
No withdrawal period is set for this drug: it is not intended for food-producing animals.3
Dispensing
Over the counter1

AVM-GSL: Authorised Veterinary Medicine - General Sale List. No prescription is needed and it may be sold by any retailer.12

Supplied without a prescription. As stated in the registration decision.

Animal species
Dogs1
Active substance
Fenbendazole
ATCvet code
QP52AC133
Manufacturer
Marketing authorisation holder: C&H Generics Ltd

Withdrawal period

No withdrawal period is set for this drug: it is not intended for food-producing animals.3

Summary of product characteristics

Composition

Each sachet contains:

Active substance:

Fenbendazole 888.8 mg

Excipient(s):

For the full list of excipients, see section 6.1.

6.1 List of excipients

Lactose monohydrate

Povidone

Sodium laurilsulfate

3

Pharmaceutical form

Granules

A free flowing white to greyish white granular powder

3

Pharmacological properties

Anthelminthics (Benzimidazoles and related substances) ATC code: QP52AC13

5.1 Pharmacodynamic properties

Contains fenbendazole which is a member of the benzimidazole family of anthelmintics and has been in veterinary use for a number of years. It acts against parasites by disrupting the formation of microtubules by binding to tubulin in parasitic intestinal cells hence preventing the absorption of glucose, and as a result the parasites are gradually starved to death. Fenbendazole displays preference for parasitic as opposed to mammalian tubulin; this appears to be due to the fact that the formation of the parasitic tubulin-fenbendazole complex is more favourable kinetically under physiological conditions than the mammalian complex.

5.2 Pharmacokinetic particulars

Fenbendazole is only partly absorbed from the intestine and reaches maximum plasma concentration in dogs 4 - 9 hours after oral administration.

Fenbendazole and its metabolites are distributed throughout the body but highest concentrations are found in the liver.

Fenbendazole is metabolised mainly by enzymes of the cytochrome P-450 system in the liver. The major oxidative metabolite is fenbendazole sulfoxide which is further metabolised to fenbendazole sulfone.

Fenbendazole and its metabolites are predominantly excreted via the faeces.

3

Target species

Dogs.

3

Indications

Dogs

For the treatment of immature and mature stages of Toxacara canis and Taenia hydatigena.

3

Dosage

For oral administration only; sprinkled onto food.

For the routine treatment of adult dogs a dosage of 100 mg/kg is recommended. This equates to approximately 1 whole sachet per 8 kg bodyweight (2 sachets for 16 kg bodyweight; 3 sachets for 24 kg bodyweight etc.).

Sachets must not be divided and stored for future use. If necessary, a suitable alternative product must be selected.

To ensure administration of a correct dose, body weight should be determined as accurately as possible.

3

Contraindications

Do not use in cases of hypersensitivity to the active substance, or to any of the excipients.

3

Adverse reactions

None known

3

Warnings

Special precautions for use in animals

Not applicable

Special precautions to be taken by the person administering the veterinary medicinal product to animals

Embryotic effects cannot be excluded. Pregnant women must take extra precautions when handling this product.

This product may be toxic to humans after ingestion. Accidental ingestion of the product should be avoided. In the event of accidental ingestion, rinse mouth with plenty of clean water and seek medical advice.

The product can cause irritation to the skin, eyes and lungs. Avoid contact with skin and/or eyes. Avoid inhalation of granule dust. When handling and applying to food, care should be taken to avoid direct contact with the skin and eyes and inhalation of dust. Wash hands after use. In case of accidental skin and/or eye contact, immediately rinse with plenty of clean water. If irritation persists, seek medical advice. Only use for the bodyweight of animal recommended. The entire contents of the sachet must be directly sprinkled onto food as a single dose. Discard any uneaten medicated feed immediately.

3

Use during pregnancy, lactation or lay

The use is not recommended during pregnancy or lactation.

Use only according to the benefit/risk assessment by the responsible veterinarian.

3

Interactions

None known.

3

Overdose

Benzimidazoles have a wide margin of safety.

3

Special warnings

None

3

Withdrawal period

Not applicable.

3

Incompatibilities

In the absence of compatibility studies, this veterinary medicinal product must not be mixed with other veterinary medicinal products.

3

Immediate packaging

Sachet consisting of paper, low density polyethylene and foil containing 4g of granules, with a heat-seal closure.

Each carton contains 1, 2, 3, 4 or 5 sachets.

Not all pack sizes may be marketed.

3

Storage

Store in a dry place.

Add to feed immediately before administration. Discard any remaining medicated feed.

3

Shelf life

Shelf life of the veterinary medicinal product as packaged for sale: 3 years.

3

Disposal of unused product

Any unused veterinary medicinal product or waste materials derived from such veterinary medicinal products should be disposed of in accordance with local requirements

3

Additional information

Vm 40162/4006

9 DATE OF FIRST AUTHORISATION

02 December 2016

10 DATE OF REVISION OF THE TEXT

January 2022

Approved 10 January 2022

3

Registration holder

C&H Generics Ltd c/o Michael McEvoy and Co.

Seville House

New Dock Street

Galway

Ireland

3

Regulations

Sources

  1. VMD Product Information Database: Ridaworm Wormer Granules 888 mg for Adult Dogs (Fenbendazole), 40162/4006 UK Veterinary Medicines Directorate (OGL v3.0), checked 2026-10-04 archived copy from 2026-10-04
  2. The Veterinary Medicines Regulations 2013, Schedule 3 (categories of veterinary medicinal products) UK Government, legislation.gov.uk, checked 2026-10-04 archived copy from 2026-10-04
  3. Summary of Product Characteristics: Ridaworm Wormer Granules 888 mg for Adult Dogs (Fenbendazole) UK Veterinary Medicines Directorate, SPC of the marketing authorisation holder, checked 2026-10-04 archived copy from 2026-10-04

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