Article 3 F1

medicated feedingstuffs as defined in Council Directive 90/167/EEC of 26 March 1990 laying down the conditions governing the preparation, placing on the market and use of medicated feedingstuffs in the Community ^f1 ;

inactivated immunological veterinary medicinal products which are manufactured from pathogens and antigens obtained from an animal or animals from a holding and used for the treatment of that animal or the animals of that holding in the same locality;

veterinary medicinal products based on radio-active isotopes;

any additives covered by Council Directive 70/524/EEC of 23 November 1970 concerning additives in feedingstuffs ^f2 where they are incorporated in animal feedingstuffs and supplementary animal feedingstuffs in accordance with that Directive; and

without prejudice to Article 95, medicinal products for veterinary use intended for research and development trials.

any medicinal product prepared in a pharmacy in accordance with a veterinary prescription for an individual animal or a small group of animals, commonly known as the magistral formula; and

any medicinal product prepared in a pharmacy in accordance with the prescriptions of a pharmacopoeia and intended to be supplied directly to the end-user, commonly known as the officinal formula.