FDA Accepts Zingo(TM) Supplemental New Drug Application To Reduce Pain Associated With Peripheral Needle Insertion Procedures In Adults

Anesiva, Inc. (Nasdaq: ANSV) announced that the U.S. Food and Drug Administration (FDA) has accepted the company’s electronic supplemental New Drug Application (sNDA) filing to expand the indication for Zingo to treat pain associated with peripheral IV insertions and blood draws in adults.

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Filed under: Pain / Anesthetics on May 22nd, 2008