Regulation 1994/2701 - Amendment of Annexes I, II, III and IV 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

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1.

Current status

This regulation was in effect from January  7, 1995 until July  5, 2009.

2.

Key information

official title

Commission Regulation (EC) No 2701/94 of 7 November 1994 amending Annexes I, II, III and IV 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
 
Legal instrument Regulation
Number legal act Regulation 1994/2701
CELEX number i 31994R2701

3.

Key dates

Document 07-11-1994
Publication in Official Journal 08-11-1994; Special edition in Finnish: Chapter 03 Volume 062,Special edition in Lithuanian: Chapter 03 Volume 016,Special edition in Swedish: Chapter 03 Volume 062,Special edition in Romanian: Chapter 03 Volume 016,Special edition in Latvian: Chapter 03 Volume 016,Special edition in Polish: Chapter 03 Volume 016,OJ L 287, 8.11.1994,Special edition in Slovenian: Chapter 03 Volume 016,Special edition in Estonian: Chapter 03 Volume 016,Special edition in Hungarian: Chapter 03 Volume 016,Special edition in Bulgarian: Chapter 03 Volume 016,Special edition in Slovak: Chapter 03 Volume 016,Special edition in Maltese: Chapter 03 Volume 016,Special edition in Czech: Chapter 03 Volume 016
Effect 07-01-1995; Entry into force Date pub. + 60 See Art 2
End of validity 05-07-2009; Implicitly repealed by 32009R0470

4.

Legislative text

8.11.1994   

EN

Official Journal of the European Communities

L 287/7

 

COMMISSION REGULATION (EC) NO 2701/94

of 7 November 1994

amending Annexes I, II, III and IV 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

(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), as last amended by Commission Regulation (EC) No 1430/94 (2), and in particular Articles 6, 7 and 8 thereof,

Whereas, since the adoption of the Regulation, the Annexes have been amended a number of times; whereas, by reason of their number, their complexity and their dispersal among various Official Journals of the European Communities, the texts are difficult to use and thus lack the clarity which should be an essential feature of all legislation; whereas, they should therefore be consolidated; whereas on the same occasion the name or chemical description of some compounds should be rectified or made more precise and certain material errors should be corrected;

Whereas the measures provided for in this Regulation are in accordance with the opinion of the Committee for the adaptation to technical progress of directives on the removal of technical barriers to trade in the veterinary medicinal products sector,

HAS ADOPTED THIS REGULATION:

Article 1

Annexes I, II, III and IV to Regulation (EEC) No 2377/90 are hereby amended as set out in the Annex hereto.

Article 2

This Regulation shall enter into force on the 60th day following its publication in the Official Journal of the European Communities.

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

Done at Brussels, 7 November 1994.

For the Commission

Martin BANGEMANN

Member of the Commission

 

 

ANNEX

ANNEX I

List of pharmacologically active substances for which maximum residue limits have been fixed

 

1.

Anti-infectious agents

 

1.1.

Chemotherapeutics

 

1.1.1.

Sulfonamides

 

Pharmacologically active substance(s)

Marker residue

Animal species

MRLs

Target tissues

Other provisions

All substances belonging to the sulfonamide group

Parent drug

All food producing species

100 μg/kg

Muscle, liver, kidney, fat

The combined total residues of all substances within the sulfonamide group should not exceed 100 μg/kg

 

1.2.

Antibiotics

 

1.2.1.

Penicillins

 

Pharmacologically active substance(s)

Marker residue

Animal species

MRLs

Target tissues

Other provisions

1.2.1.1.

Benzylpenicillin

Benzylpenicillin

All food producing species

50 μg/kg

Muscle, liver, kidney, fat

 

4 μg/kg

Milk

 

1.2.1.2.

Ampicillin

Ampicillin

All food producing species

50 μg/kg

Muscle, liver, kidney, fat

 

4 μg/kg

Milk

 

1.2.1.3.

Amoxicillin

Amoxicillin

All food producing species

50 μg/kg

Muscle, liver, kidney, fat

 

4 μg/kg

Milk

 

1.2.1.4.

Oxacillin

Oxacillin

All food producing species

300 μg/kg

Muscle, liver, kidney, fat

 

30 μg/kg

Milk

 

1.2.1.5.

Cloxacillin

Cloxacillin

All food producing species

300 μg/kg

Muscle, liver, kidney, fat

 

30...


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This text has been adopted from EUR-Lex.

 

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