P&U's Azulfidine EN-tabs Approved In USA

4 November 1996

- Pharmacia & Upjohn has received marketing approval from the US Food and Drug Administration for its Azulfidine EN-tabs (sulfasalazine delayed-release tablets), for the treatment of rheumatoid arthritis in patients who are unresponsive to or intolerant of to other analgesics or non-steroidal anti-inflammatory drugs. The product is already marketed in 43 countries for this indication, and is also available in the USA for the treatment of ulcerative colitis. Side effects include anorexia, nausea, vomiting and reversible low sperm count. Patients should undergo blood counts and urinalysis if receiving this medication, says the company.

This article is accessible to registered users, to continue reading please register for free.  A free trial will give you access to exclusive features, interviews, round-ups and commentary from the sharpest minds in the pharmaceutical and biotechnology space for a week. If you are already a registered user please login. If your trial has come to an end, you can subscribe here.

Login to your account

Become a subscriber

 

£820

Or £77 per month

Subscribe Now
  • Unfettered access to industry-leading news, commentary and analysis in pharma and biotech.
  • Updates from clinical trials, conferences, M&A, licensing, financing, regulation, patents & legal, executive appointments, commercial strategy and financial results.
  • Daily roundup of key events in pharma and biotech.
  • Monthly in-depth briefings on Boardroom appointments and M&A news.
  • Choose from a cost-effective annual package or a flexible monthly subscription
The Pharma Letter is an extremely useful and valuable Life Sciences service that brings together a daily update on performance people and products. It’s part of the key information for keeping me informed

Chairman, Sanofi Aventis UK



Companies featured in this story

More ones to watch >


Today's issue

Company Spotlight