Provisional Consent to the Distribution of a New Medicine Pursuant to section 23 of the Medicines Act 1981, the Minister of Health hereby consents to the distribution inNew Zealand of the new medicine set out in the Schedule hereto: Schedule Name and Strength Form Name and Address of Manufacturer Proprietary Name(if any) Pralidoxime iodide 500 mg in 200 mL Injection (ampoule) Abbott Australasia Pty Limited, Kurnell, New South Wales, Australia Pralidoxime Iodide Note: This medicine may only be distributed, supplied, or used under conditions to be imposed from time to time by the Director-General of Health. Dated this 29th day of September 1995. KAREN O. POUTASI, Director-General of Health, pursuant to delegation given by the Minister of Health on 25 June 1993.