Medicinal products on prescription only3

Subject to article 6, the following descriptions and classes of medicinal products are specified for the purposes of section 58, namely–

a

medicinal products consisting of or containing a substance listed in column 1 of Schedule 1;

b

medicinal products that are controlled drugs;

c

medicinal products that are for parenteral administration, other than preparations of insulin for parenteral administration;

d

cyanogenetic substances, other than preparations for external use;

e

medicinal products that on administration emit radiation, or contain or generate any substance which emits radiation, in order that radiation may be used;

f

medicinal products for human use which are classified as subject to medical prescription in marketing authorizations granted under Council Regulation 2309/9316;

g

medicinal products–

i

which are not of a description and do not fall within a class specified in subparagraphs (a) to (f),

ii

which are of a description in respect of which the conditions specified in section 59(1) are satisfied, and

iii

in respect of which a product licence or marketing authorization has been granted which contains a provision to the effect that the method of sale or supply of the medicinal product is to be only in accordance with a prescription given by an appropriate practitioner.