Generics firms take on Merck & Co's Pepcid

16 April 2001

Merck & Co has finally lost patent protection on its gastrointestinaldrug Pepcid (famotidine) in the USA, with a string of companies now launching generic equivalents onto the market. In addition to Mylan, which received a tentative approval from the US Food and Drug Administration to market 20mg and 40mg famotidine tablets in February, Teva, IVAX Laboratories and Pharmaceutical Resources' subsidiary Par Pharmaceutical have all indicated they will immediately launch generics. Merck achieved turnover with Pepcid of $569 million in 2000, and launched a new formulation last year, Pepcid Complete (famotidine/calcium carbonate), to help reduce the impact of the patent expiry.

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