Choose the experimental features you want to try

This document is an excerpt from the EUR-Lex website

Document 32004R1101R(01)

Corrigendum to Commission Regulation (EC) No 1101/2004 of 10 June 2004 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 (OJ L 211, 12.6.2004)

OJ L 337, 13.11.2004, p. 73–73 (ES, CS, DA, DE, ET, EL, EN, FR, IT, LV, LT, HU, NL, PL, PT, SK, SL, FI, SV)

ELI: http://data.europa.eu/eli/reg/2004/1101/corrigendum/2004-11-13/oj

13.11.2004   

EN

Official Journal of the European Union

L 337/73


Corrigendum to Commission Regulation (EC) No 1101/2004 of 10 June 2004 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

( Official Journal of the European Union L 211 of 12 June 2004 )

In the Annex, on page 5, point A is replaced as follows:

‘A.   The following substance(s) is(are) inserted in Annex I (List of pharmacologically active substances for which maximum residue limits have been fixed).

1.   Anti-infectious agents

1.2.   Antibiotics

1.2.4.   Macrolides

Pharmacologically active substance(s)

Marker residue

Animal species

MRLs

Target tissues

“Tulathromycin

(2R,3S,4R,5R,8R,10R,11R,12S, 13S,14R)-2-ethyl-3,4,10,13-tetrahydroxy-3,5,8,10,12,14-hexamethyl-11-[[3,4,6-trideoxy-3-(dimethylamino)-ß-D-xylo-hexopy-ranosyl]oxy]-1-oxa-6-azacyclopent-decan-15-one expressed as tulathromycin equivalents

Bovine (1)

100  μg/kg

Fat

3 000  μg/kg

Liver

3 000  μg/kg

Kidney

Porcine

100  μg/kg

Skin + fat

3 000  μg/kg

Liver

3 000  μg/kg

Kidney” ’


(1)  Not for use in animals from which milk is produced for human consumption.


Top