Pink Sheet is part of Pharma Intelligence UK Limited

This site is operated by Pharma Intelligence UK Limited, a company registered in England and Wales with company number 13787459 whose registered office is 5 Howick Place, London SW1P 1WG. The Pharma Intelligence group is owned by Caerus Topco S.à r.l. and all copyright resides with the group.

This copy is for your personal, non-commercial use. For high-quality copies or electronic reprints for distribution to colleagues or customers, please call +44 (0) 20 3377 3183

Printed By

UsernamePublicRestriction

FDA Approves Teva’s Generic Zoloft

This article was originally published in The Pink Sheet Daily

Executive Summary

Teva received FDA final approval for its generic version of Pfizer's antidepressant Zoloft (sertraline) June 30

Teva received FDA final approval for its generic version of Pfizer's antidepressant Zoloft (sertraline) June 30.

The generic company plans to launch the product in the "latter part of July." Teva holds 180-day marketing exclusivity for the 25 mg, 50 mg and 100 mg versions.

Pfizer said it will launch an authorized generic through its Greenstone subsidiary "if and when Zoloft becomes subject to generic competition," (1 (Also see "Pfizer Prepares For Zoloft Authorized Generic Entry Following Teva’s Launch" - Pink Sheet, 29 Jun, 2006.)).

Related Content

Topics

Latest Headlines
See All
UsernamePublicRestriction

Register

PS064429

Ask The Analyst

Ask the Analyst is free for subscribers.  Submit your question and one of our analysts will be in touch.

Your question has been successfully sent to the email address below and we will get back as soon as possible. my@email.address.

All fields are required.

Please make sure all fields are completed.

Please make sure you have filled out all fields

Please make sure you have filled out all fields

Please enter a valid e-mail address

Please enter a valid Phone Number

Ask your question to our analysts

Cancel