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Document 32006R0006

Commission Regulation (EC) No 6/2006 of 5 January 2006 amending Annexes I and II to Council Regulation (EEC) No 2377/90 laying down a Community procedure for the establishment of maximum residue limits of veterinary medicinal products in foodstuffs of animal origin, as regards dihydrostreptomycin, tosylchloramide sodium and Piceae turiones recentes extractum (Text with EEA relevance)

OJ L 3, 6.1.2006, p. 3–5 (ES, CS, DA, DE, ET, EL, EN, FR, IT, LV, LT, HU, NL, PL, PT, SK, SL, FI, SV)
OJ L 338M, 17.12.2008, p. 275–277 (MT)
Special edition in Bulgarian: Chapter 03 Volume 068 P. 149 - 151
Special edition in Romanian: Chapter 03 Volume 068 P. 149 - 151

Legal status of the document No longer in force, Date of end of validity: 05/07/2009; Implicitly repealed by 32009R0470

ELI: http://data.europa.eu/eli/reg/2006/6/oj

Date of document:
05/01/2006
Date of effect:
09/01/2006; Entry into force Date pub. + 3 See Art 2
Date of effect:
07/03/2006; Application See Art 2
Date of end of validity:
05/07/2009; Implicitly repealed by 32009R0470
Author:
European Commission
Form:
Regulation
Additional information:
Extended to the EEA by 22006D0116, EEA relevance
Authentic language:
Spanish, Czech, Danish, German, Estonian, Greek, English, French, Italian, Latvian, Lithuanian, Hungarian, Maltese, Dutch, Polish, Portuguese, Slovak, Slovenian, Finnish, Swedish, Icelandic, Norwegian
Treaty:
Treaty establishing the European Community
Legal basis:
Link
Link
Link
Select all documents mentioning this document
Modifies:
Relation Act Comment Subdivision concerned From To
Modifies 31990R2377 Amendment annex 1 01/03/2006
Modifies 31990R2377 Amendment annex 2 01/03/2006
Modified by:
Relation Act Comment Subdivision concerned From To
Corrected by 32006R0006R(01) (MT)
Implicitly repealed by 32009R0470 06/07/2009
Instruments cited:
Link
Link

6.1.2006   

EN

Official Journal of the European Union

L 3/3

COMMISSION REGULATION (EC) No 6/2006

of 5 January 2006

amending Annexes I and II to Council Regulation (EEC) No 2377/90 laying down a Community procedure for the establishment of maximum residue limits of veterinary medicinal products in foodstuffs of animal origin, as regards dihydrostreptomycin, tosylchloramide sodium and Piceae turiones recentes extractum

(Text with EEA relevance)

THE COMMISSION OF THE EUROPEAN COMMUNITIES,

Having regard to the Treaty establishing the European Community,

Having regard to Council Regulation (EEC) No 2377/90 of 26 June 1990 laying down a Community procedure for the establishment of maximum residue limits of veterinary medicinal products in foodstuffs of animal origin (1), and in particular Articles 2 and 3 thereof,

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

Whereas:

(1)

All pharmacologically active substances which are used within the Community in veterinary medicinal products intended for administration to food-producing animals should be evaluated in accordance with Regulation (EEC) No 2377/90.

(2)

Dihydrostreptomycin has been included in Annex I to Regulation (EEC) No 2377/90 for bovine and ovine species, for muscle, fat, liver, kidney and milk, and for porcine species for muscle, liver, kidney and skin and fat in natural proportions. That entry should be extended from bovine and ovine species to all ruminants.

(3)

Tosylchloramide has been included in Annex II to Regulation (EEC) No 2377/90 for fin fish for water borne only and for bovine for topical use only. That entry should be extended to Equidae for topical use only.

(4)

An application for establishing of maximum residue limits for Piceae turiones recentes extractum has been submitted. This substance should be included in Annex II to that Regulation for all food producing species for oral use only.

(5)

Regulation (EEC) No 2377/90 should be amended accordingly.

(6)

An adequate period should be allowed before the applicability of this Regulation in order to enable Member States to make any adjustment which may be necessary in the light of this Regulation to the marketing authorisations granted in accordance with Directive 2001/82/EC of the European Parliament and of the Council of 6 November 2001 on the Community code relating to veterinary medicinal products (2).

(7)

The measures provided for in this Regulation are in accordance with the opinion of the Standing Committee on Veterinary Medicinal Products,

HAS ADOPTED THIS REGULATION:

Article 1

Annexes I and II to Regulation (EEC) No 2377/90 are amended in accordance with the Annex to this Regulation.

Article 2

This Regulation shall enter into force on the third day following that of its publication in the Official Journal of the European Union.

It shall apply from 7 March 2006.

This Regulation shall be binding in its entirety and directly applicable in all Member States.

Done at Brussels, 5 January 2006.

For the Commission

Günter VERHEUGEN

Vice-President

(1)   OJ L 224, 18.8.1990, p. 1. Regulation as last amended by Commission Regulation (EC) No 1911/2005 (OJ L 305, 24.11.2005, p. 30).

(2)   OJ L 311, 28.11.2001, p. 1. Directive as last amended by Directive 2004/28/EC (OJ L 136, 30.4.2004, p. 58).

ANNEX

A.   The following substance is inserted in Annex I to Regulation (EEC) No 2377/90:

1.   Anti-infectious agents

1.2.   Antibiotics

1.2.10.   Aminoglycosides

Pharmacologically active substance(s)

Marker residue

Animal species

MRLs

Target tissues

‘Dihydrostreptomycin

Dihydrostreptomycin

all ruminants

500  μg/kg

Muscle

500  μg/kg

Fat

500  μg/kg

Liver

1 000  μg/kg

Kidney

200  μg/kg

Milk’

B.   The following substances are inserted in Annex II to Regulation (EEC) No 2377/90:

2.   Organic compounds

Pharmacologically active substance(s)

Animal species

‘Tosylchloramide sodium

Equidae (1)

6.   Substances of vegetable origin

Pharmacologically active substance(s)

Animal species

‘Piceae turiones recentes extractum

All food producing species (2)

(1)  For topical use only.’

(2)  For oral use only.’

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