Veterinary Medicines Information website

BYEMITE 500 MG/ML CONCENTRATE FOR SPRAYING EMULSION FOR LAYING HENS

Authorised

Phoxim

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Product identification

Medicine name:

BYEMITE 500 MG/ML CONCENTRATE FOR SPRAYING EMULSION FOR LAYING HENS

Active substance:

Phoxim

Target species:

Chicken (layer hen)

Route of administration:

Cutaneous use

Product details

Active substance and strength:

Phoxim

500.00

milligram(s)

/

1.00

millilitre(s)

Pharmaceutical form:

Concentrate for spray emulsion

Withdrawal period by route of administration:

Cutaneous use
- Chicken (layer hen)
  - Meat and offal
    
    25
    
    day
    
    Remove eggs before treatment. Discard eggs laid during and on the same day after the treatment.
    Meat and offal: 25 days after the second treatment.
  - Eggs
    
    12
    
    hour
    
    Remove eggs before treatment. Discard eggs laid during and on the same day after the treatment.

Anatomical therapeutic chemical veterinary (ATCvet) codes:

QP53AF01

Legal status of supply:

Veterinary medicinal product subject to veterinary prescription

Authorisation status:

Valid

Authorised in:

Belgium

Available in:

Belgium

Package description:

Available only in French
Available only in French
Available only in French

Additional information

Entitlement type:

Marketing Authorisation

Legal basis of product authorisation:

Generic application (Article 13(1) of Directive No 2001/82/EC)

Marketing authorisation holder:

Elanco Animal Health GmbH

Marketing authorisation date:

18/02/2009

Manufacturing sites for batch release:

KVP Pharma+Veterinaer Produkte GmbH

Responsible authority:

Federal Agency For Medicines And Health Products

Authorisation number:

BE-V333837

Date of authorisation status change:

18/02/2009

Reference member state:

France

Procedure number:

FR/V/0196/001

Concerned member states:

Austria
Belgium
Bulgaria
Cyprus
Czechia
Finland
Greece
Hungary
Iceland
Ireland
Italy
Luxembourg
Netherlands
Portugal
Romania
Slovakia
Slovenia
Sweden

To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet

Documents

Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.

Other languages (2)

French (PDF)

Published on: 30/10/2025

Dutch (PDF)

Published on: 30/10/2025

Package Leaflet

This document does not exist in this language (English). You can find it in another language below.

Other languages (3)

French (PDF)

Published on: 30/10/2025

German (PDF)

Published on: 30/10/2025

Dutch (PDF)

Published on: 30/10/2025

Labelling

This document does not exist in this language (English). You can find it in another language below.

Other languages (3)

French (PDF)

Published on: 13/03/2026

German (PDF)

Published on: 13/03/2026

Dutch (PDF)

Published on: 13/03/2026

Package Leaflet and Labelling

This document does not exist in this language (English). You can find it in another language below.

Other languages (3)

French (PDF)

Published on: 30/10/2025

German (PDF)

Published on: 30/10/2025

Dutch (PDF)

Published on: 30/10/2025

Combined File of all Documents

English (PDF)

Published on: 13/03/2026