Commission Regulation (EC) No 1464/2004 of 17 August 2004 concerning the authorisation for 10 years of the additive «Monteban» in feedingstuffs, belonging to the group of coccidiostats and other medicinal substances(Text with EEA relevance)
Modified by
  • Commission Regulation (EC) No 545/2006of 31 March 2006amending Regulation (EC) No 1464/2004 as regards the conditions for authorisation of the feed additive Monteban, belonging to the group of coccidiostats and other medicinal substances(Text with EEA relevance), 306R0545, April 1, 2006
Commission Regulation (EC) No 1464/2004of 17 August 2004concerning the authorisation for 10 years of the additive Monteban in feedingstuffs, belonging to the group of coccidiostats and other medicinal substances(Text with EEA relevance) THE COMMISSION OF THE EUROPEAN COMMUNITIES,Having regard to the Treaty establishing the European Community,Having regard to Council Directive 70/524/EEC of 23 November 1970 concerning additives in feedingstuffsOJ L 270, 14.12.1970, p. 1. Directive as last amended by Commission Regulation (EC) No 1289/2004 (OJ L 243, 15.7.2004, p. 15)., and in particular Article 9g(5)(b) thereof,Whereas:(1)In accordance with Directive 70/524/EEC, coccidiostats included in Annex I to that Directive before 1 January 1988 were provisionally authorised as from 1 April 1998 and transferred to Chapter I of Annex B with a view to their re-evaluation as additives linked to a person responsible for putting them into circulation. The narasin product, Monteban, is an additive belonging to the group "Coccidiostats and other medicinal substances" listed in Chapter I of Annex B to Directive 70/524/EEC.(2)The person responsible for putting into circulation Monteban submitted an application for authorisation and a dossier, according to Article 9g(2) and (4) of that Directive.(3)Article 9g(6) of Directive 70/524/EEC allows the automatic extension of the period of authorisation of the additives concerned until the Commission takes a decision in cases where, for reasons beyond the control of the authorisation holder, no decision may be taken on the application before the expiry date of the authorisation. This provision is applicable to the authorisation of Monteban. The Commission requested a full risk evaluation from the Scientific Committee for Animal Nutrition on 26 April 2001 and this request was consequently transferred to the European Food Safety Authority. Several requests for additional information were made during the re-evaluation process, making it impossible to complete the re-evaluation within the time limits required by Article 9g.(4)The Scientific Panel on Additives and Products or Substances used in Animal Feed attached to the European Food Safety Authority has delivered a favourable opinion with regard to the safety and to the efficacy of Monteban for chickens for fattening.(5)The re-evaluation of Monteban carried out by the Commission showed that the relevant conditions laid down in Directive 70/524/EEC are satisfied. Monteban should therefore be authorised for 10 years as an additive linked to the person responsible for putting it into circulation and included in Chapter I of the list referred to Article 9t(b) of that Directive.(6)As the authorisation for the additive is now linked to a person responsible for putting it into circulation, and replaces the previous authorisation which was not linked to any specific person, it is appropriate to delete the latter authorisation.(7)Since there are no safety reasons for withdrawing the product narasin from the market immediately, it is appropriate to allow a transitional period of six months for the disposal of existing stocks of the additive.(8)The measures provided for in this Regulation are in accordance with the opinion of the Standing Committee on the Food Chain and Animal Health,HAS ADOPTED THIS REGULATION:
Article 1Chapter I of Annex B to Directive 70/524/EEC is amended as follows:the additive narasin, belonging to the group "Coccidiostats and other medical substances", is deleted.
Article 2The additive Monteban belonging to the group "Coccidiostats and other medical substances", as set out in the Annex to the present Regulation, is authorised for use in animal nutrition under the conditions laid down in that Annex.
Article 3A period of six months from the date of entry into force of this Regulation is permitted to use up the existing stocks of narasin.
Article 4This Regulation shall enter into force on the third day following that of its publication in the Official Journal of the European Union.
This Regulation shall be binding in its entirety and directly applicable in all Member States.ANNEX
Coccidiostats and other medicinal substances
Registration number of additiveName and registration number of person responsible for putting additive into circulationAdditive(Trade name)Composition, chemical formula, descriptionSpecies or category of animalMaximum ageMinimum contentMaximum contentOther provisionsEnd of period of authorisationMaximum residue limits (MRLs) in the relevant foodstuffs of animal origin from species or category of animal concerned
mg of active substance/kg of complete feedingstuff
E 765Eli Lilly and Company LimitedNarasin 100 g/kg(Monteban, Monteban G 100)Additive composition:Narasin: 100 g activity/kgSoybean oil or mineral oil: 10-30 g/kgVermiculite: 0-20 g/kgSoybean mill run or rice hulls qs 1 kgActive substance:Narasin, C43H72O11CAS number: 55134-13-9polyether monocarboxylic acid produced by Streptomyces aureofaciens (NRRL 8092), in granular formNarasin A activity: ≥ 90 %Chickens for fattening—6070Use prohibited at least one day before slaughter.Indicate in the instructions for use:"Dangerous for equine species, turkeys and rabbits""This feedingstuff contains an ionophore: simultaneous use with certain medicinal substances (e.g. tiamulin) can be contraindicated"21.8.201450 μg Narasin/kg for all wet tissues from chickens for fattening