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Axcan Receives FDA Approval Letter for PYLERA'TM' -Formerly Known as HELIZIDE-, an Innovative 3-in-1 Capsule Triple Therapy for the Eradication of Helicobacter Pylori.
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Canadian Corporate News
- Article date:
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September 29, 2006
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Copyright informationCOPYRIGHT 2006 Canadian Corporate News. News Provided by Comtex. This material is published under license from the publisher through the Gale Group, Farmington Hills, Michigan. All inquiries regarding rights should be directed to the Gale Group. (Hide copyright information)
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MONT-SAINT-HILAIRE, QUEBEC, Sep 29, 2006 (CCNMatthews via COMTEX) -- Axcan Pharma Inc. (TSX:AXP)(NASDAQ:AXCA) today announced that the US Food and Drug Administration ("FDA") has issued an approval letter for the Company's New Drug Application for PYLERA(TM) (formerly HELIZIDE). PYLERA(TM) is a patented 3-in-1 capsule triple therapy, for the eradication of Helicobacter pylori, which is a bacterium now recognized as being the main cause of gastric and duodenal ulcers. Each PYLERA(TM) capsule contains biskalcitrate potassium (140 mg), metronidazole (125 mg) and tetracycline hydrochloride (125 mg). The U.S. patent on the PYLERA(TM) capsule technology expires in December 2018.
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