Open AccessModification of the terms of the authorisation regarding the formulation of Maxiban ® G160 (narasin and nicarbazin) for chickens for fattening
Author(s) -
Rychen Guido,
Aquilina Gabriele,
Azimonti Giovanna,
Bampidis Vasileios,
Lourdes Bastos Maria,
Bories Georges,
Chesson Andrew,
Cocconcelli Pier Sandro,
Flachowsky Gerhard,
Kolar Boris,
Kouba Maryline,
López Puente Secundino,
LópezAlonso Marta,
Mantovani Alberto,
Mayo Baltasar,
Ramos Fernando,
Saarela Maria,
Villa Roberto Edoardo,
Wallace Robert John,
Wester Pieter,
Brantom Paul,
Halle Ingrid,
Beelen Patrick,
Holczknecht Orsolya,
Vittoria Vettori Maria,
Gropp Jürgen
Publication year - 2016
Publication title -
efsa journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.076
H-Index - 97
ISSN - 1831-4732
DOI - 10.2903/j.efsa.2016.4614
Subject(s) - authorization , european commission , feed additive , animal feed , zoology , european union , coccidiostats , microbiology and biotechnology , veterinary medicine , biology , medicine , business , coccidiosis , computer science , computer security , economic policy , broiler
Following a request from European Commission, the Panel on Additives and Products or Substances used in Animal Feed ( FEEDAP ) was asked to deliver a scientific opinion on the proposed modification of the terms of the authorisation regarding the formulation of the product Maxiban ® G160 (narasin and nicarbazin). The applicant has proposed to modify the concentration of Microtracer‐F‐Red in the additive from the currently authorised 11 g/kg to a range of 4–11 g/kg. Based on data submitted on the composition and the stability, the FEEDAP Panel concluded that the physicochemical properties of the additive were not affected by the proposed modification. Therefore, the assessment of safety and efficacy made for the former formulation with 11 g Microtracer‐F‐Red/kg is still valid for the newly applied formulation.