Commission Implementing Regulation (EU) No 123/2012 of 13 February 2012 amending the Annex to Regulation (EU) No 37/2010 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin, as regards the substance monepantel Text with EEA relevance

Type Implementing Regulation
Publication 2012-02-14
State In force
Text As published
Department European Commission
Source EUR-Lex
articles 2

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14.2.2012 EN Official Journal of the European Union L 40/4

THE EUROPEAN COMMISSION,

Having regard to the Treaty on the Functioning of the European Union,

Having regard to Regulation (EC) No 470/2009 of the European Parliament and of the Council of 6 May 2009 laying down Community procedures for the establishment of residue limits of pharmacologically active substances in foodstuffs of animal origin, repealing Council Regulation (EEC) No 2377/90 and amending Directive 2001/82/EC of the European Parliament and of the Council and Regulation (EC) No 726/2004 of the European Parliament and the Council [^ntr1-L_2012040EN.01000401-E0001], and in particular Article 14 in conjunction with Article 17 thereof,

Having regard to the opinion of the European Medicines Agency formulated by the Committee for Medicinal Products for Veterinary Use,

Whereas:

HAS ADOPTED THIS REGULATION:

Article 1

The Annex to Regulation (EU) No 37/2010 is amended as set out in the Annex to this Regulation.

Article 2

This Regulation shall enter into force on the third day following 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, 13 February 2012.

For the Commission

The President

José Manuel BARROSO

[^ntr1-L_2012040EN.01000401-E0001]: OJ L 152, 16.6.2009, p. 11.

[^ntr2-L_2012040EN.01000401-E0002]: OJ L 15, 20.1.2010, p. 1.

ANNEX

The entry monepantel in Table 1 of the Annex to Regulation (EU) No 37/2010 is replaced by the following:

Pharmacologically active Substance Marker residue Animal Species MRL Target Tissues Other Provisions (according to Article 14(7) of Regulation (EC) No 470/2009) Therapeutic Classification
‘Monepantel Monepantel-sulfone Ovine, caprine 700 μg/kg Muscle Not for use in animals producing milk for human consumption. Antiparasitic agents/Agents acting against endoparasites’
‘Monepantel Monepantel-sulfone Ovine, caprine 7 000  μg/kg Fat Not for use in animals producing milk for human consumption. Antiparasitic agents/Agents acting against endoparasites’
‘Monepantel Monepantel-sulfone Ovine, caprine 5 000  μg/kg Liver Not for use in animals producing milk for human consumption. Antiparasitic agents/Agents acting against endoparasites’
‘Monepantel Monepantel-sulfone Ovine, caprine 2 000  μg/kg Kidney Not for use in animals producing milk for human consumption. Antiparasitic agents/Agents acting against endoparasites’

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