Notice Type
Departmental
Consent to the Distribution of a Changed Medicine Pursuant to section 20 of the Medicines Act 1981, the Minister of Health hereby consents to the distribution in New Zealand of the changed medicine which was referred to the Minister of Health under the provisions of section 24 (5) of the Act and are set out in the Schedule hereto: Schedule Name and Strength Form Name and Address of Manufacturer Proprietary Name(if any) Amifostine 500 mg Injection, powder Ben Venue Laboratories Inc., Bedford, Ohio, United States of America; and USB Pharma BV., Nijmegen, The Netherlands Ethyol Dated this 13th day of May 1999. G. R. BOYD, Chief Advisor, Regulation and Safety, pursuant to delegation given by the Minister of Health on the 20th day of February 1997.
Publication Date
20 May 1999

Notice Number

1999-go3596

Page Number

1347