EAST WINDSOR, N.J.--(BUSINESS WIRE)--NexMed, Inc. (Nasdaq: NEXM), a developer of innovative transdermal products based on its proprietary NexACT® drug delivery technology, today announced that it filed the New Drug Application (NDA) for its topically applied alprostadil cream for the treatment of erectile dysfunction with the U.S. Food and Drug Administration (FDA) on September 21, 2007. The FDA customarily accepts or refuses an NDA and designates review status within sixty (60) days of filing. Once accepted, the standard review time by the FDA is twelve (12) months.
