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Commission Regulation (EC) No. 205/2006 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 toltrazuril, diethylene glycol monoethyl ether and polyoxyethylene sorbitan monooleate.

Country
Type of law
Regulation
Source

Abstract
All pharmacologically active substances used within the Community in veterinary medicinal products intended for administration to animals for the purpose of producing foodstuffs must be evaluated in accordance with Regulation (EEC) No. 2377/90. Annexes I and II to that Regulation are supplemented by inserting certain veterinary medicinal products (namely toltrazuril, diethylene glycol monoethyl ether and polyoxyethylene sorbitan monooleate) and their respective maximum residue limits in the list of pharmacologically active substances.
Date of text
Repealed
Yes
Serial Imprint
Official Journal of the European Union L 34, 7 February 2006, pp. 21-23.
Source language

English

Legislation Amendment
Yes