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Paragraph 5 F1

A liquid formulation—

(a)

containing a botanical extract of cannabis—

(i)

with a concentration of not more than 30 milligrams of cannabidiol per millilitre, and not more than 30 milligrams of delta-9-tetrahydrocannabinol per millilitre, and

(ii)

where the ratio of cannabidiol to delta-9-tetrahydrocannabinol is between 0.7 and 1.3,

(b)

which is dispensed through a metered dose pump as a mucosal mouth spray, and

(c)

which was approved for marketing by the Medicines and Healthcare Products Regulatory Agency on 16th June 2010

Annotations

Textual amendments

F1

Sch. 4 Pt. 1 para. 5 inserted (10.4.2013) by The Misuse of Drugs (Amendment No. 2) (England, Wales and Scotland) Regulations 2013 (S.I. 2013/625), regs. 1(1), 7