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Regulation (EU) 2019/4 of the European Parliament and of the Council of 11 December 2018 on the manufacture, placing on the market and use of medicated feed, amending Regulation (EC) No 183/2005 of the European Parliament and of the Council and repealing Council Directive 90/167/EEC (Text with EEA relevance) article annex_IV CELEX: 32019R0004 PERMITTED TOLERANCES FOR THE COMPOSITIONAL LABELLING OF MEDICATED FEED OR INTERMEDIATE PRODUCTS AS REFERRED TO IN ARTICLE 9(3)
The tolerances laid down in this Annex shall only include technical deviations.
Where the composition of a medicated feed or an intermediate product is found to deviate from the amount of an antimicrobial active substance indicated on the label, a tolerance of 10 % shall apply.
For the other active substances, the following tolerances shall apply:
Active substance per kg of medicated feed or intermediate products Tolerance > 500 mg ± 10 % ≤ 500 mg ± 20 % |