Veterinary Medicine Information website

VETBUTON 100 MG/ML SOLUTION FOR INJECTION FOR CATTLE, PIGS, HORSES, SHEEP AND GOATS

Authorised
  • Menbutone
Download as PDF

Product identification

Medicine name:
VETBUTON 100 MG/ML SOLUTION FOR INJECTION FOR CATTLE, PIGS, HORSES, SHEEP AND GOATS
Active substance:
  • Menbutone
Target species:
  • Goat
  • Pig
  • Sheep
  • Cattle
  • Horse
Route of administration:
  • Intramuscular use
  • Intravenous use

Product details

Active substance and strength:
  • Menbutone
    100.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Goat
      • Meat and offal
        0
        day
      • Milk
        0
        day
    • Pig
      • Meat and offal
        0
        day
    • Sheep
      • Meat and offal
        0
        day
      • Milk
        0
        day
  • Intravenous use
    • Cattle
      • Meat and offal
        0
        day
      • Milk
        0
        day
    • Pig
      • Meat and offal
        0
        day
    • Horse
      • Meat and offal
        0
        day
      • Milk
        0
        day
    • Sheep
      • Meat and offal
        0
        day
      • Milk
        0
        day
    • Goat
      • Meat and offal
        0
        day
      • Milk
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QA05AX90
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Belgium
Available in:
  • Belgium
Package description:
  • Cardboard box with one 100 ml natural multi-layer (COEX) PP/EVOH/PP vial closed with bromobutyl rubber stopper and aluminium and plastic flip capsule.

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:
  • Przedsiebiorstwo Wielobranzowe Vet-Agro Sp. z o.o.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Przedsiebiorstwo Wielobranzowe Vet-Agro Sp. z o.o.
Responsible authority:
  • Federal Agency For Medicines And Health Products
Authorisation number:
  • BE-V544782
Date of authorisation status change:
Reference member state:
  • France
Procedure number:
  • FR/V/0324/001
Concerned member states:
  • Belgium
  • Croatia
  • Netherlands
  • Portugal
  • Romania
  • Slovenia
  • Spain
  • Sweden

Documents

Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
French (PDF)
Published on: 17/08/2025
Download
German (PDF)
Published on: 17/08/2025
Download
Dutch (PDF)
Published on: 17/08/2025
Download

Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
French (PDF)
Published on: 17/08/2025
Download
German (PDF)
Published on: 17/08/2025
Download
Dutch (PDF)
Published on: 17/08/2025
Download

Labelling

This document does not exist in this language (English). You can find it in another language below.
French (PDF)
Published on: 17/08/2025
Download
German (PDF)
Published on: 17/08/2025
Download
Dutch (PDF)
Published on: 17/08/2025
Download

Combined File of all Documents

English (PDF)
Published on: 14/03/2026
Download

eu-puar-frv0324001-mr-rpe522-en.pdf

English (PDF)
Published on: 13/03/2026
Download