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Eli Lilly and Company

FDA Approves Lilly's ZYPREXA RELPREVV for Treatment of Schizophrenia in Adults

Published in Medical Letter on the CDC and FDA, January 3rd, 2010

The U.S. Food and Drug Administration (FDA) approved ZYPREXA RELPREVV (olanzapine) For Extended Release Injectable Suspension for the treatment of schizophrenia in adults, Eli Lilly and Company (NYSE:LLY) announced. ZYPREXA RELPREVV, a long-acting intramuscular injection, sustains the delivery of olanzapine for up to four weeks.

Different from both oral and injected short-acting formulations, long-acting formulations of antipsychotics allow for stable concentrations of the active drug to remain at a therapeutic range for an extended period of time.(i)

"Patients, families and communities often needlessly suffer the consequences of relapse when daily...

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