Panacur Small Animal 100 mg/ml Oral Suspension
Fenbendazole
Last verified
Veterinary medicinal product: oral suspension. Distribution category: NFA-VPS (Veterinary Medicines Regulations 2013, Schedule 3). Active substance: Fenbendazole.1
In short: questions and answers
- Does Panacur Small Animal 100 mg/ml Oral Suspension need a prescription?
- Over the counter. As stated in the registration decision.1
- Which animals is Panacur Small Animal 100 mg/ml Oral Suspension for?
- Cats, Dogs.1
- What is the active substance in Panacur Small Animal 100 mg/ml Oral Suspension?
- Fenbendazole. ATCvet code: QP52AC13.13
- What is the withdrawal period of Panacur Small Animal 100 mg/ml Oral Suspension 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
NFA-VPS: Non-Food Animal - Veterinarian, Pharmacist, Suitably Qualified Person. For animals not kept for food. No prescription is needed, but it is supplied only by a veterinary surgeon, a pharmacist or a suitably qualified person (SQP).12
Supplied without a prescription. As stated in the registration decision.
- Active substance
- Fenbendazole
- ATCvet code
- QP52AC133
- Manufacturer
- Marketing authorisation holder: Intervet International B.V.
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 ml contains:
Active substance:
Fenbendazole 100 mg
Excipients:
| Qualitative composition of excipients and other constituents | Quantitative composition if that information is essential for proper administration of the veterinary medicinal product |
|---|---|
| Benzyl alcohol | 4.835 mg |
| Sodium methyl parahydroxybenzoate | 2.000 mg |
| Sodium propyl parahydroxybenzoate | 0.216 mg |
| Silica, colloidal anhydrous | |
| Povidone K25 | |
| Carmellose sodium | |
| Sodium citrate dihydrate | |
| Citric acid monohydrate | |
| Purified water |
White to off white suspension.
Pharmacological properties
4.1 ATCvet code: QP52AC13
4.2 Pharmacodynamics
Fenbendazole is an anthelmintic belonging to the benzimidazole carbamates group. It acts by interfering in the energy metabolism of the nematode. The anthelmintic efficacy is based on inhibition of the polymerisation of tubulin to microtubuli. The anthelmintic affects both adult and immature stages of gastrointestinal and respiratory nematodes.
4.3 Pharmacokinetics
Fenbendazole is only partly absorbed after oral administration and is then metabolised in the liver. Fenbendazole and its metabolites are distributed throughout the body and high concentrations can be found in the liver. The elimination of fenbendazole and its metabolites occurs primarily via the faeces (> 90%) and to a small extent in the urine and milk.
Fenbendazole is metabolised to its sulphoxide, then to sulphone and amines.
Target species
Dogs, cats, puppies and kittens.
Indications
A broad spectrum anthelmintic for the treatment of domestic dogs and cats infected with immature and mature stages of nematodes of the gastrointestinal and respiratory tracts.
Adult dogs and cats: For the treatment of adult dogs and cats infected with gastrointestinal nematodes and cestodes:
Ascarid spp. (Toxocara canis, Toxocara cati , Toxascaris leonina)
Ancylostoma spp.
Trichuris spp.
Uncinaria spp.
Taenia spp.
Puppies and kittens: For the treatment of puppies and kittens infected with gastrointestinal nematodes and puppies infected with protozoa (Giardia spp.).
Pregnant dogs: For the treatment of pregnant dogs to reduce prenatal infections with Toxocara canis and the transfer of T.canis and Ancylostoma caninum to their pups via the milk.
Also for the treatment of domestic dogs infected with lungworm Oslerus (Filaroides) osleri or protozoa Giardia spp., and cats infected with lungworm Aelurostrongylus abstrusus.
Also has an ovicidal effect on nematode eggs.
Dosage
Oral use.
Shake container before use.
Routine treatment of adult dogs and cats
1 ml per 1 kg body weight as a single oral dose. (= 100 mg fenbendazole/kg body weight)
Practical dosage recommendations:
| Body weight | Dose |
|---|---|
| 2 to 4 kg | 4 ml |
| 4 to 8 kg | 8 ml |
| 8 to 16 kg | 16 ml |
| 16 to 24 kg | 24 ml |
| 24 to 32 kg | 32 ml |
| 32 to 64 kg | 64 ml |
For dogs weighing over 64 kg, an extra 10 ml are required for each additional 10 kg body weight.
The dose should be added to feed, directly before feeding or administered by mouth directly after feeding.
Treatment should be repeated when natural re-infection with parasitic worms occurs. Routine treatment of adult animals with minimal exposure to infection is advisable 2 to 4 times per year. More frequent treatment at 6 to 8 weekly intervals is advisable for dogs in kennels.
Puppies and kittens under 6 months of age
0.5 ml per kg body weight daily for 3 consecutive days given by mouth directly after feeding to unweaned animals or added to feed for weaned animals, directly before feeding. (= 50 mg fenbendazole/kg body weight daily for 3 days)
Practical dosage recommendations:
Up to 1 kg | 0.5 ml daily for 3 days
1 to 2 kg | 1 ml daily for 3 days
2 to 4 kg | 2 ml daily for 3 days
4 to 6 kg | 3 ml daily for 3 days
6 to 8 kg | 4 ml daily for 3 days
8 to 10 kg | 5 ml daily for 3 days
For puppies weighing over 10 kg, an extra 0.5 ml is required daily for each additional kg body weight.
Puppies should be treated at 2 weeks of age, 5 weeks of age and again before leaving the breeder's premises. Treatment may also be required at 8 and 12 weeks of age. Thereafter, frequency of treatment can be reduced unless the pups remain in kennels where reinfection occurs more readily.
Pregnant dogs
1 ml per 4 kg body weight daily from day 40 of pregnancy continuously to 2 days post-whelping (approximately 25 days) (= 25 mg fenbendazole/kg body weight daily).
Practical dosage recommendations:
4 kg | 1 ml daily for approx. 25 days
8 kg | 2 ml daily for approx. 25 days
12 kg | 3 ml daily for approx. 25 days
20 kg | 5 ml daily for approx. 25 days
40 kg | 10 ml daily for approx. 25 days
For dogs weighing over 40 kg, an extra 1 ml is required daily for each additional 4 kg body weight.
As treatment of pregnant dogs is 98 % effective, puppies from these dogs should themselves be treated with a 3 day course at 2 and 5 weeks of age.
Pregnant cats
Pregnant cats can be safely treated but only require a single treatment at the routine adult dose rate. Administer 1ml per kg body weight as a single dose. (= 100mg fenbendazole/kg body weight)
Increased dosing for specific infections
For the treatment of clinical worm infestations in adult dogs and cats or Giardia spp. infections in dogs, administer 1 ml per 2 kg body weight daily for 3 consecutive days. (= 50 mg fenbendazole/kg body weight daily for 3 days)
For the control of lungworm Oslerus (Filaroides) osleri in dogs administer 1 ml per 2 kg body weight for 7 consecutive days. (= 50 mg fenbendazole/kg body weight daily for 7 days) A repeat course of treatment may be required in some cases.
For the control of lungworm Aelurostrongylus abstrusus in cats administer 1 ml per 2 kg body weight for 3 consecutive days. (= 50 mg fenbendazole/kg body weight daily for 3 days)
To ensure a correct dosage, body weight should be determined as accurately as possible.
Contraindications
None.
Adverse reactions
Dogs, cats, puppies and kittens:
| Very rare (<1 animal / 10,000 animals treated, including isolated reports): | Gastrointestinal disorders (e.g. vomiting or diarrhoea). |
|---|
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.
Warnings
Special precautions for safe use in the target species:
Assess body weight as accurately as possible before calculating the dosage.
Special precautions to be taken by the person administering the veterinary medicinal product to animals:
Direct contact with the skin should be kept to a minimum.
Personal protective equipment consisting of impermeable rubber gloves should be worn when handling the veterinary medicinal product.
Wash hands thoroughly with soap and water after use.
Special precautions for the protection of the environment:
Not applicable.
3.11 Special restrictions for use and special conditions for use, including restrictions on the use of antimicrobial and antiparasitic veterinary medicinal products in order to limit the risk of development of resistance
Not applicable.
Use during pregnancy, lactation or lay
Pregnancy:
The product can be used in pregnant bitches.
As teratogenic effects in dogs and cats cannot be completely ruled out in very rare cases, the treatment in the first two trimesters of pregnancy should be based on the benefit-risk evaluation by the responsible veterinary surgeon.
Interactions
None known.
Overdose
Benzimidazoles have a high margin of safety.
No specific overdose symptoms are known. No specific action is required.
Special warnings
The use of the veterinary medicinal product should be based on local epidemiological information about susceptibility of the nematodes and recommendations on how to limit further selection for resistance to anthelmintics.
Withdrawal period
Not applicable.
Incompatibilities
None known.
Immediate packaging
Cardboard box with 1 x 100 ml multidose bottle.
Container: Opaque or solid white high density polyethylene bottle.
Closure: Foil seal with a polyethylene or polypropylene screw cap.
Storage
Do not freeze.
Shelf life
Shelf life of the veterinary medicinal product as packaged for sale: 2 years.
Disposal of unused product
Medicines should not be disposed of via wastewater.
The veterinary medicinal product should not enter water courses as fenbendazole may be dangerous for fish and other aquatic organisms.
Use take-back schemes for the disposal of any unused veterinary medicinal product or waste materials derived thereof in accordance with local requirements and with any national collection systems applicable to the veterinary medicinal product concerned.
Additional information
Vm 06376/4077
8 DATE OF FIRST AUTHORISATION
29 January 1993
9 DATE OF THE LAST REVISION OF THE SUMMARY OF THE PRODUCT CHARACTERISTICS
July 2025
10 CLASSIFICATION OF VETERINARY MEDICINAL PRODUCT
Veterinary medicinal product not subject to prescription.
Find more product information by searching for the ‘Product Information Database’ on www.gov.uk.
Approved: 17 October 2025
Registration holder
Intervet International B.V.
Regulations
- Veterinary Medicines Regulations 2013 (SI 2013/2033), Schedule 32
Sources
- VMD Product Information Database: Panacur Small Animal 100 mg/ml Oral Suspension, 06376/4077
- The Veterinary Medicines Regulations 2013, Schedule 3 (categories of veterinary medicinal products)
- Summary of Product Characteristics: Panacur Small Animal 100 mg/ml Oral Suspension
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