Commission Implementing Regulation (EU) 2015/46 of 14 January 2015 concerning the authorisation of diclazuril as a feed additive for chickens for fattening, for turkeys for fattening and for guinea fowl for fattening and breeding (holder of authorisation Huvepharma NV) (Text with EEA relevance)
Grade B
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Address https://gelex.eu/eli/EU/regulation/2015/46@2015-01-14/en
THE EUROPEAN COMMISSION,
Having regard to the Treaty on the Functioning of the European Union,
Having regard to Regulation (EC) No 1831/2003 of the European Parliament and of the Council of 22 September 2003 on additives for use in animal nutrition, and in particular Article 9(2) thereof,
Whereas:
(1) Regulation (EC) No 1831/2003 provides for the authorisation of additives for use in animal nutrition and for the grounds and procedures for granting such authorisation.
(2) In accordance with Article 7 of Regulation (EC) No 1831/2003 an application was submitted for the authorisation of a preparation of diclazuril. That application was accompanied by the particulars and documents required under Article 7(3) of Regulation (EC) No 1831/2003.
(3) That application concerns the authorisation of diclazuril, CAS number 101831-37-2, as a feed additive for chickens for fattening, for turkeys for fattening and for guinea fowl for fattening and breeding, to be classified in the additive category coccidiostats and histomonostas.
(4) The European Food Safety Authority (the Authority) concluded in its opinions of 21 May 2014, 22 May 2014 that, under the proposed conditions of use, diclazuril does not have an adverse effect on animal health, human health or the environment and it is effective in controlling coccidiosis in chickens for fattening, turkeys for fattening and guinea fowl for fattening and breeding. The Authority does not consider that there is a need for specific requirements of post-market monitoring. It also verified the report on the method of analysis of the feed additive in feed submitted by the Reference Laboratory set up by Regulation (EC) No 1831/2003.
(5) The assessment of diclazuril, CAS number 101831-37-2, shows that the conditions for authorisation, as provided for in Article 5 of Regulation (EC) No 1831/2003, are satisfied. Accordingly, the use of that preparation should be authorised as specified in the Annex to this Regulation.
(6) The measures provided for in this Regulation are in accordance with the opinion of the Standing Committee on Plants, Animals, Food and Feed,
HAS ADOPTED THIS REGULATION:
Article 1 Authorisation
Diclazuril, CAS number 101831-37-2, belonging to the additive category coccidiostats and histomonostas, is authorised as an additive in animal nutrition, subject to the conditions laid down in that Annex.
Article 2
This Regulation shall enter into force on the twentieth 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. Done at Brussels, 14 January 2015. For the Commission The President Jean-Claude Juncker
ANNEX
ANNEX
Identification number of the additive Name of the holder of authorisation Additive Composition, chemical formula, description, analytical method Species or category of animal Maximum age Minimum content Maximum content Other provisions End of period of authorisation Maximum Residue Limits (MRLs) in the relevant foodstuffs of animal origin mg of active substance/kg of complete feedingstuff with a moisture content of 12 % Coccidiostats and histomonostats 51775 Huvepharma NV. Diclazuril 0,5 g/100 g (Coxiril) Chickens for fattening Turkeys for fattening Guinea fowl for fattening and for breeding — 0,8 1,2 4 February 2025 Regulation (EU) No 37/2010
Additive composition
Diclazuril: 5 g/kg. Starch: 15 g/kg. Wheat meal: 700 g/kg. Calcium carbonate: 280 g/kg.
Characterisation of the active substance
Diclazuril, C17H9Cl3N4O2, (±)-4-chlorophenyl[2,6-dichloro-4- (2,3,4,5- tetrahydro-3,5-dioxo-1,2,4-triazin-2- yl)phenyl]acetonitrile, CAS number: 101831-37-2. Impurity D: ≤ 0,1 %. Any other single impurity: ≤ 0,5 %. Total impurities: ≤ 1,5 %.
Analytical method
For determination of diclazuril in feed: reversed-phase high performance liquid chromatography (HPLC) using Ultraviolet detection at 280nm (Regulation (EC) No 152/2009).
1. The additive shall be incorporated in compound feed in the form of a premixture.
2. Diclazuril shall not be mixed with other coccidiostats.
3. For safety: breathing protection, glasses and gloves shall be used during handling.
4. A post-market monitoring programme concerning the resistance to bacteria and Eimeria spp. shall be carried out by the holder of authorisation.
1500μg diclazuril/kg of wet liver;
1000 μg diclazuril/kg of wet kidney;
500 μg diclazuril/kg of wet muscle;
500 μg diclazuril/kg of wet skin/fat.
Versions
Cited by
- Commission Implementing Regulation (EU) 2023/2733 of 7 December 2023 concerning the authorisation of a preparation of diclazuril (Coxiril) as a feed additive for chickens reared for laying and pheasants (holder of authorisation: Huvepharma NV) and correcting Implementing Regulation (EU) 2015/46 (Text with EEA relevance) Regulation · Grade B
The preparation of diclazuril (Coxiril) is already authorised as a feed additive for chickens for fattening, turkeys for fattening, as well as guinea fowls for fattening and breeding by Commission Implementing Regulation (EU) 2015/46.
- Commission Implementing Regulation (EU) 2023/2733 of 7 December 2023 concerning the authorisation of a preparation of diclazuril (Coxiril) as a feed additive for chickens reared for laying and pheasants (holder of authorisation: Huvepharma NV) and correcting Implementing Regulation (EU) 2015/46 (Text with EEA relevance) Regulation · Grade B
In the last column of the Annex to Implementing Regulation (EU) 2015/46, on maximum residue limits (MRLs) in the relevant foodstuffs of animal origin, reference is made to Regulation (EU) No 37/2010 and the MRLs are also detailed. However, in accordance with article 9(7) of Regulation (EC) No 1831/2003, where an MRL has already been established for a substance under Community rules, that MRL shall also apply to residues of the active substance or its metabolites originating from the use of the substance as a feed additive. The MRLs established in Regulation (EU) No 37/2010 for diclazuril in po
- Commission Implementing Regulation (EU) 2023/2733 of 7 December 2023 concerning the authorisation of a preparation of diclazuril (Coxiril) as a feed additive for chickens reared for laying and pheasants (holder of authorisation: Huvepharma NV) and correcting Implementing Regulation (EU) 2015/46 (Text with EEA relevance) Regulation · Grade B
In the Annex to Implementing Regulation (EU) 2015/46, the text in the column Maximum residue limits (MRLs) in the relevant foodstuffs of animal origin is replaced by the following: Regulation (EU) No 37/2010.