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4. The following descriptions or classes of medicinal products are specified for the purposes of section 58 of the Act—
(a)veterinary drugs specified in Schedule 1;
(b)veterinary drugs which contain controlled drugs;
(c)veterinary drugs for parenteral administration which do not fall within paragraph (a) or (b) above;
(d)veterinary drugs—
(i)which do not fall within paragraph (a), (b) or (c) above; and
(ii)in respect of which there is a marketing authorisation granted or varied after 30th March 2001 in accordance with an application containing a provision to the effect that the method of sale or supply of the veterinary drug in question is to be only in accordance with a prescription given by an appropriate practitioner; and
(e)veterinary drugs granted a marketing authorisation, in accordance with the provisions of Council Regulation (EEC) No. 2309/93 (laying down Community procedures for the authorisation and supervision of medicinal products for human and veterinary use and establishing a European Agency for the Evaluation of Medicinal Products(1)), after the coming into force of this Order.
OJ No. L214, 24.8.93, p.1.
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