Drug product labeling for Zoloft (Sertraline)

Robert Groves made this Official Information request to Ministry of Health

Response to this request is long overdue. By law Ministry of Health should have responded by now (details and exceptions). You can complain to the Ombudsman.

From: Robert Groves

Dear Ministry of Health,

Pursuant to NZ’s Official Information Act, I would like to submit this Application for Product Information (PI) documents, product lableing documents, product monograph, and/or leaflet from the Ministry of Health (or Medsafe) regarding Zoloft (Sertraline) in 50mg or 100mg tablet/other form, dating from the Zoloft’s first registration with the Ministry of Health to its most current edition.

As you may know, sometimes Zoloft may be referred to as “Lustral.”

Yours faithfully,

R. Groves

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Ministry of Health

Dear Mr Groves

Thank you for your request for official information, received by the
Ministry of Health on 14 April 2014.

Your request has been received and logged.  As required under the Official
Information Act 1982, the Ministry will respond to your request within 20
working days.  You should receive a response on or before 15 May 2014.

If a large amount of information has been requested or if the Ministry
needs to consult in order to make a decision, we may need to extend this
date (this is provided for in section 15A of the Act).  We will advise you
if such an extension is necessary.

The Ministry's reference number for your request is: H201401521.

Yours sincerely
 
Government Relations
Corporate Services
Ministry of Health
[1]mailto:[email address]

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