Article 4 Medicinal products on prescription only

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^f1), after the coming into force of this Order.

Annotations

Footnotes

f1: OJ No. L214, 24.8.93, p.1.