OpenLegislation

Paragraph 10 Incorporation of a medicinal premix into feedingstuffsF4E1

England, Wales and Scotland

Any person who incorporates a F1medicinal premix (or F2an intermediate feedingstuff) into feedingstuffs—

(a)

must do so in accordance with the summary of product characteristics, and must take account of any interactions listed there;

(b)

must ensure that the medicinal premix does not contain the same active substance as any other additive;

(c)

must ensure that the medicinal premix is incorporated in accordance with its marketing authorisation (unless it has been prescribed under the cascade) and the F3medicated feedingstuff prescription;

(d)

must ensure that the daily dose of the medicinal premix is contained in a quantity of medicated feedingstuffs corresponding to at least half the daily feedingstuffs ration of the animals treated or, in the case of ruminants, corresponding to at least half the daily requirements of non-mineral complementary feedingstuffs.

Annotations

Textual amendments

F1

Words in Sch. 5 para. 10 substituted (E.W.S.) (17.5.2024) by The Veterinary Medicines (Amendment etc.) Regulations 2024 (S.I. 2024/567), regs. 1(1), 132(a)

F2

Words in Sch. 5 para. 10 substituted (E.W.S.) (17.5.2024) by The Veterinary Medicines (Amendment etc.) Regulations 2024 (S.I. 2024/567), regs. 1(1), 132(b)

F3

Words in Sch. 5 para. 10(c) substituted (E.W.S.) (17.5.2024) by The Veterinary Medicines (Amendment etc.) Regulations 2024 (S.I. 2024/567), regs. 1(1), 132(c)

F4

Words in Sch. 5 para. 10 heading substituted (E.W.S.) (17.5.2024) by The Veterinary Medicines (Amendment etc.) Regulations 2024 (S.I. 2024/567), regs. 1(1), 132(d)

Extent

E1

This version of this provision extends to England and Wales and Scotland only; a separate version has been created for Northern Ireland only