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POM-V Prescription Required

Amphen 200 mg/g Granules for Use in Drinking Water for Pigs

Active ingredient: Florfenicol

Form

Powder

Species

Pigs

Manufacturer

Huvepharma NV

VMD MA No.

30282/4043

What it's used for

the disease must be established in the group before metaphylactic treatment.

Full indications, dosage and side effects ↓
View official SPC (PDF)

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Paying less for Florfenicol

  1. 1

    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.

  2. 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.

Prescription required

Your vet must provide a written prescription on request. You can then purchase from any licensed online retailer.

Clinical information

Amphen 200 mg/g Granules for Use in Drinking Water for Pigs — SPC Details

Source: VMD Summary of Product Characteristics (SPC). Last updated 27 Mar 2026.

the disease must be established in the group before metaphylactic treatment.
10 mg florfenicol/kg bodyweight per day in drinking water for 5 consecutive days.
The daily amount of veterinary medicinal product to be mixed with drinking water can be
calculated based on the Total Body Weight (TBW) of the group to be treated with the
following formula:
Total Body Weight of the group (TBW) in kgAmount of veterinary
medicinal product (in grams)
per day*
=
* to be mixed with the estimated total water consumption of the group in 24 hours.
The examples of medicated drinking water in the table below are calculated by applying
the formula and by assuming that pigs drink 8% or 10% of their bodyweight.
TBW of the
group (kg
Veterinary
medicinal
product (g)
Estimated daily
water
consumption (L)
Veterinary
medicinal
product grams
per 10 litres of
water
Pigs drinking 500 kg25 g40 L

Revised December 2024
AN: 00622/2024 & 00623/2024
1000 kg50 g80 L8% of their
bodyweight
5000 kg250 g400 L6.25 g/10 L500 kg25 g50 L1000 kg50 g100 LPigs drinking
10%
bodyweight
5000 Kg250 g500 L
5 g/10 L

The maximum solubility of the veterinary medicinal product granules is 2.5 g/L at 10 °C
and 20 °C and 2.0 g/L at 5 °C. Dissolution may take up to 30 minutes. During
dissolution the solution should be stirred for at least 5 minutes at 50 RPM. Solutions
should be checked visually for complete dissolution.
FOR BULK TANK:
Any solution for use in a header tank must be limited to not more than the maximum
solubility.
FOR PROPORTIONER:
For stock solutions and when using a proportioner, take care not to exceed the
maximum solubility which can be achieved under the given conditions. Adjust flow rate
settings of the dosing pump according to concentration of the stock solution and water
intake of the animals to be treated.
To treat 5,000 kg of pigs, drinking 10% of their bodyweight, at the dose rate of
10 mg/kg:
1. Fill the proportioner with 100 L drinking water (temperature not below 10
°C).
2. Add 250 g of veterinary medicinal product to the proportioner.
3. Mix thoroughly until visually dissolved.
4. Set the proportioner to 20%.
5. Turn on the proportioner.
In order to ensure correct dosing and to prevent underdosing, the body weight of the
group should be calculated as precisely as possible and water consumption should be
monitored. The required quantity of granules should be measured by suitably calibrated
weighing equipment.
The uptake of water depends on several factors including the age, the clinical state of
the animals and the local conditions such as ambient temperature and humidity. The
daily water consumption can be underestimated (e.g. reduced to 6% of bodyweight) in
order to ensure total consumption of medicated water during the day (fresh drinking
water can be made available following the consumption of the medicated water). If it is
not possible to obtain sufficient uptake of medicated water animals should be treated
parenterally.
Medicated drinking water should be replaced every 24 hours.
Do not administer to boars intended for breeding purposes.
Do not use in cases of hypersensitivity to the active substance or to any of the
excipients.
Do not use in case of known resistance to florfenicol.

Revised December 2024
AN: 00622/2024 & 00623/2024
Very commonDiarrhoea
Revised December 2024
AN: 00622/2024 & 00623/2024
(>1 animal / 10 animals treated):Erythema
1,2
, Oedema
1,2
.
Very rare
(<1 animal / 10,000 animals
treated, including isolated
reports):
Rectal prolapse
.Undetermined frequency (cannot
be estimated from the available
data):
Decreased drinking
, Inappetence
Unusual stool colour
, Constipation.
transient,
peri-anal or rectal,
resolves without treatment,
slight,
dark brown
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.
In case of insufficient water intake, animals should be treated parenterally. During
treatment, unmedicated drinking water should only be administered after the daily
amount of medicated drinking water has been ingested by pigs. The veterinary
medicinal product is not intended to be used together with other antibiotics.

Special precautions for safe use in the target species:
Use of the veterinary medicinal product should be based on susceptibility testing of the
bacteria isolated from the animal. If this not possible, therapy should be based on local
(regional, farm level) epidemiological information about susceptibility of the target
bacteria.
Official and local antimicrobial policies should be taken into account when the veterinary
medicinal product is used.
Use of the veterinary medicinal product deviating from the instructions given in the SPC
may increase the prevalence of bacteria resistant to florfenicol and may decrease the
effectiveness of treatment with amphenicols due to the potential for cross-resistance.
Treatment should not exceed 5 days. During treatment, increased serum calcium may
also be observed.
Do not use the veterinary medicinal product with chlorinated water.
Special precautions to be taken by the person administering the veterinary medicinal
product to animals:
This veterinary medicinal product may cause hypersensitivity reactions. People with
known hypersensitivity to florfenicol, polysorbate 80 or polyethylene glycol should avoid
contact with the veterinary medicinal product. Personal protective equipment consisting
of protective gloves, safety glasses and clothing should be worn when handling the
veterinary medicinal product. If you develop symptoms following exposure such as skin
rash, seek medical advice immediately and show the package leaflet or the label to the
physician.
This veterinary medicinal product may be slightly irritating to the eyes and/or skin. Avoid
contact with the skin and eyes, including hand-to-eye-contact. Wear safety glasses. In
case of accidental spillage onto eyes, wash them immediately with water. In case of
contact with the skin, wash immediately the affected area and take the contaminated
clothes off.
This veterinary medicinal product may be harmful after ingestion. Do not smoke, eat or
drink when handling the veterinary medicinal product or mixing the medicated drinking
water.
Special precautions for the protection of the environment:
Manure from treated animals may be harmful to terrestrial plants.
None known.
Store in the original container in order to protect from light.
Meat and offal: 20 days.

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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