Fenbendazole - maximum residue limit

fenbendazole

About

The maximum residue limit (MRL) is the maximum allowed concentration of residue in a food product from an animal that has received a veterinary medicine or that has been exposed to a biocidal product for use in animal husbandry.

Documents

Opinion of the CVMP on the establishment of maximum residue limits: Fenbendazole

Adopted Reference Number: EMA/CVMP/845730/2011

Fenbendazole: European public maximum-residue-limit assessment report (EPMAR) - CVMP

Adopted Reference Number: EMA/CVMP/914694/2011

Fenbendazole (extrapolation to all ruminants): Summary report (4) - Committee for Veterinary Medicinal Products

Reference Number: EMEA/MRL/866/03-FINAL

Oxfendazole, fenbendazole, febantel: Summary report (2) - Committee for Veterinary Medicinal Products

Adopted

Fenbendazole: Summary report (3) - Committee for Veterinary Medicinal Products

Reference Number: EMEA/MRL/193/97/-FINAL

Oxfendazole, fenbendazole, febantel: Summary report (1) - Committee for Veterinary Medicinal Products

Adopted

Document description:

• Summary opinion of the CVMP on the establishment of maximum residue limits - A summary opinion on the MRL for those substances for which a recommendation is made to the European Commission
• Opinion of the CVMP on the establishment of maximum residue limits – Full opinion following the publication of the Commission Regulation formally establishing the MRL status
• European public maximum residue limit assessment report (EPMAR) – Detailed information on the CVMP’s evaluation following the publication of the Commission Regulation
• Summary report – Superseded title for the documents which are now called EPMAR

Key facts

• Active substance:
  fenbendazole
• Therapeutic classification:
  Agents (acting) against endoparasites
• Target species:
  All food producing species except fin fish
• Date of Commission implementing decision:
  1 February 2012
• Commission implementing regulation:
  Regulation (EU) 1161/2012