Pursuant to section 35(1)(a) of the Medicines Act 1981, the Minister of Health hereby revokes consent to the distribution in New Zealand of the medicine:
Prexige (lumiracoxib) 200mg film-coated tablets
Prexige (lumiracoxib) 400mg film-coated tablets
Dated this 16th day of August 2007.
COLIN FEEK, Acting Director-General of Health (pursuant to the delegation given by the Minister of Health on 27 June 2001).