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Tequin Approved By FDA, Available By Year End PRINCETON, NJ -- December 21, 1999 -- Bristol-Myers Squibb has announced that the U.S. Food and Drug Administration approved its New Drug Application for Tequin(TM) (gatifloxacin), in bioequivalent 400mg oral and IV formulations. Tequin is a a broad-spectrum quinolone antibiotic and will be available for physicians to prescribe before the end of the year. Related Link: Bristol-Myers Squibb. E-mail this page to a friend or colleague! To print, use this version