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Wednesday, November 5th, 2008...10:37 pm

Depomed Doses First Patient In New Phase 3 Clinical Trial Of Gabapentin GR In Postherpetic Neuralgia Part 3

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About Depomed Depomed, Inc. is a specialty pharmaceutical business with two agreed products on the jamboree and other service claimant in its pipeline. The company utilize its proven, proprietary AcuFormTM linctus propagation technology to upgrade extant oral medication, allowing for stretched, controlled production of medications to the upper gastrointestinal tract. Benefits of AcuForm-enhanced pharmaceuticals necessitate the ease of access of once-daily direction, better analysis tolerability and enhanced deference and efficacy. GLUMETZA® (metformin hydrochloride extended release tablets) is approved for put into effect in adults with genus 2 diabetes and is person market in Canada by Biovail Corporation. ProQuin® XR (ciprofloxacin hydrochloride) extended release tablets are approved in the United States for the once-daily treatment of uncomplicated urinary tract infection and is being marketed in the United States in the urology and Ob/Gyn specialties by Watson Pharmaceuticals. Product candidate Gabapentin GR is currently in clinical initiation for the treatment of neuropathic pain and menopausal roasting flash. Additional data nearly Depomed may be found on its website, “Safe Harbor” Statement down the stairs the Private Securities Litigation Reform Act of 1995. Statements here wring release that are not historical facts are forward-looking statement that involve arbitrariness and uncertainties. The inclusion of forward-looking statements, with those connected to expectations on the subject concern of our clinical development programs and likely benefits of our products and product candidates, should not be respect by a graph that any of our cause will be finish. Actual grades may fluctuate materially from those set forth in this release in the red to the risks and uncertainties innate in our conglomerate, including, minus reduction, risks and uncertainties related to: our research and development pains, including pre-clinical and clinical conduct test; restraint by the FDA and other administration agencies; the thing of regulatory application and product launch; our dimensions to gloriously commercialize our products; the glory of our collaborative provision with development and commercialization partner; and other risks detailed in our filings with the Securities and Exchange Commission filings, including our incomparable recent Annual Report on Form 10-K. You are caution not to put undue confidence on these forward-looking statements which allege solitary commencing the date hereof. We occupy in no condition to check through or update this release to emulate activities or setting that come to run beyond after the date of this release.

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