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Commission Delegated Regulation (EU) 2024/1159 Article 9

Commission Delegated Regulation (EU) 2024/1159 Article 9

Product information

Article 9

1.   The product information of an antimicrobial or antiparasitic veterinary medicinal product to be administered to a terrestrial food-producing animal species by means of mixing into solid feed or administered on the surface of solid feed immediately prior to feeding shall clearly indicate that the product is to be administered only for the treatment of individually fed animals or a small group of animals where the intake of veterinary medicinal products by individual animals can be effectively controlled. 2.   The product information of a veterinary medicinal product to be administered orally by means of mixing into drinking water or liquid feed shall provide appropriate guidance on known interactions and incompatibilities between the veterinary medicinal product and biocidal products, feed additives or other substances used in drinking water. Where no data or information on potential interactions or incompatibilities is available, the product information shall include a warning indicating that no such information is available. 3.   Where relevant, marketing authorisation holders of veterinary medicinal products authorised before 9 November 2025 shall amend their existing marketing authorisations or product information, as appropriate, in accordance with paragraphs 1 and 2 at the latest by 9 May 2029.

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Other provisions in Commission Delegated Regulation (EU) 2024/1159

Compiled from an official source version. Later amendments or repeals may not be reflected; the official text prevails. · Read the official text ↗ · Data as of 2026-07-04

CitationArticle 9 of Commission Delegated Regulation (EU) 2024/1159 (LawPlayer, data as of 2026-07-04)

© European Union, https://eur-lex.europa.eu, 1998-2026. Reuse authorised under Commission Decision 2011/833/EU, provided the source is acknowledged.

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