Medicinal products on prescription only4

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 Products10), after the coming into force of this Order.