The Medicines (Veterinary Drugs) (Prescription Only) Order 1991
In the case of the veterinary drugs, the sale or supply shall be subject to the conditions specified in Articles 3(2) and 4(3) of the Veterinary Drugs Exemption Order.
4
Persons the sale or supply by whom is exempted by Article 3 of the Veterinary Drugs Exemption Order from the restrictions imposed by section 52.
4
Any veterinary drug such as is described in Article 3(1) of the Veterinary Drugs Exemption Order which, if or when for parenteral administration, is a prescription only medicine.
4
The sale or supply shall be subject to the conditions specified in Article 3 of the Veterinary Drugs Exemption Order.
5
Persons the sale or supply by whom is exempted by Article 6 or 9 of the Veterinary Drugs Exemption Order from the restrictions imposed by section 52.
5
Any veterinary drug such as is described in Article 6 or 9 of the Veterinary Drugs Exemption Order which is a prescription only medicine.
5
The sale or supply shall be subject to—
- (a) the presentation of an order signed by or on behalf of the purchaser stating—
- (i) the name and address of the purchaser,
- (ii) the name and address of the purchaser’s business and
- (iii) the amount of the veterinary drug required, and
- (b) the conditions specified in Article 6 or 9 of the Veterinary Drugs Exemption Order.
6
Persons providing a poultry vaccination service.
6
Any veterinary drug such as is described in Article 3(1) of the Veterinary Drugs Exemption Order which is a poultry vaccine and which, if or when for parenteral administration, is a prescription only medicine.
6
The sale or supply shall be only to a person who has charge of animals for the purpose of and in the course of carrying on a business, either as his sole business activity or as a substantial part of his business activities.
7
Person selling or supplying prescription only medicines to the persons referred to in paragraph 6.
7
The veterinary drugs referred to in paragraph 6.
7
The sale or supply shall be subject to the presentation of an order signed by the purchaser stating the amount of the prescription only medicine required.
8
Persons selling or supplying prescription only medicines to veterinary surgeons and veterinary practitioners.
8
All prescription only medicines.
8
No conditions.
9
Persons selling or supplying prescription only medicines to the British Standards Institution.
9
All prescription only medicines.
9
The sale or supply shall be–
- (a) subject to the presentation of an order signed on behalf of the British Standards Institution stating the status of the person signing it and the amount of the prescription only medicine required, and
- (b) only for the purpose of testing containers of medicinal products or determining the standards for such containers.
10
Holders of product licences and holders of manufacturer’s licences.
10
Prescription only medicines referred to in the licences.
10
the sale or supply shall be only–
- (a) to a pharmacist,
- (b) so as to enable that pharmacist to prepare an entry relating to the prescription only medicine in question in a tablet or capsule identification guide or similar publication, and
- (c) of no greater quantity than is reasonably necessary for that purpose.
PART II
1
Persons authorised by licences granted under regulation 5 of the Misuse of Drugs Regulations to supply a controlled drug.
1
Such prescription only medicines, being controlled drugs, as are specified in the licence.
1
The supply shall be subject to such conditions and in such circumstances and to such an extent as may be specified in the licence.
PART III
1
Persons providing a poultry vaccination service.
1
Any veterinary drug such as is described in Article 3(1) of the Veterinary Drugs Exemption Order which is a poultry vaccine and which, if or when for parenteral administration, is a prescription only medicine.
1
The administration shall be only in the course of providing a poultry vaccination service.
2
Persons who are authorised as members of a group by a group authority granted under regulations 8(3) or 9(3) of the Misuse of Drugs Regulations to supply a controlled drug by way of administration only.
2
Prescription only medicines that are specified in the group authority.
2
The administration shall be subject to such conditions and in such circumstances and to such extent as may be specified in the group authority.
3
Persons who have in their charge or who maintain animals for the purposes of and in the course of carrying on a business either as their sole business activity or as a part of their business activities.
3
Any veterinary drug such as is described in Article 3(1) of the Veterinary Drugs Exemption Order which, if or when for parenteral administration, is a prescription only medicine.
3
The administration shall be only to animals in their charge or under their maintenance for the purposes of and in the course of carrying on a business.
Signed
Virginia Bottomley — Minister of State for Health — 11th June 1991
Strathclyde — Parliamentary Under Secretary of State, Scottish Office — 11th June 1991
David Hunt — Secretary of State for Wales — 12th June 1991
In witness whereof the Official Seal of the Minister of Agriculture, Fisheries and Food is hereunto affixed on 10th June 1991.
John Selwyn Gummer — Minister of Agriculture, Fisheries and Food
Sealed with the Official Seal of the Department of Health and Social Services for Northern Ireland this 13th day of June 1991
F. A. Elliott — Permanent Secretary
Sealed with the Official Seal of the Department of Agriculture for Northern Ireland this 13th day of June 1991
W. J. Hodges — Permanent Secretary
Explanatory note
(This note is not part of the Order)
This Order replaces the Medicines (Veterinary Drugs) (Prescription Only) Order 1989. The Order specifies descriptions and classes of medicinal products (being veterinary drugs) for the purposes of section 58 of the Medicines Act 1968. By virtue of section 58 such products may be sold or supplied by retail only in accordance with a prescription given by a veterinary surgeon or veterinary practitioner and may be administered only by or in accordance with the directions of such a person.
This Order clarifies the definition of “strength” and “maximum strength”; in all three Schedules the quantity of the substance contained in each product is specified in terms of weight or volume.
In relation to some products specified in Schedule 1 there are some deletions and additions.
Footnotes
[^f00001]: 1968 c. 67; “the appropriate Ministers” referred to in sections 58 and 59 is defined in section 1 (see also the following footnote).
[^f00002]: In the case of the Secretaries of State concerned with health in England and in Wales by virtue of S.I. 1969/388, in the case of the Secretary of State concerned with agriculture in Wales by virtue of S.I. 1978/272 and in the case of the Northern Ireland Departments by virtue of the Northern Ireland Constitution Act 1973 (c. 36), section 40 and Schedule 5, and the Northern Ireland Act 1974 (c. 28), section 1(3) and Schedule 1, paragraph 2(1)(b).
[^f00003]: 1971 c. 38.
[^f00004]: S.I. 1985/2066; relevant amending instrument is S.I. 1986/2330.
[^f00005]: S.R.(N.I.) 1986 No. 52; relevant amending instrument is S.R.(N.I.) 1987 No. 68.
[^f00006]: S.I. 1989/2318, amended by S.I. 1990/568 and 1990/2496.
[^f00007]: S.I. 1989/2319.
[^f00008]: S.I. 1983/1212, amended by S.I. 1984/756 and 1988/2017.
[^f00009]: Additional restrictions on the retail sale or supply of products containing chloroform are imposed by the Medicines (Chloroform Prohibition) Order 1979 (S.I. 1979/382, amended by S.I. 1980/263).
[^f00010]: See also the Medicines (Phenacetin Prohibition) Order 1979 (S.I. 1979/1181).
[^f00011]: 1990 c. 16.
[^f00012]: S.I. 1991 No. 762 (N.I.7).
[^f00013]: 1970 c. 40.
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