Healthcare Industry News:  alprostadil 

Biopharmaceuticals Drug Delivery FDA

 News Release - September 24, 2007

NexMed Files NDA for Proprietary Erectile Dysfunction Treatment

EAST WINDSOR, N.J.--(HSMN NewsFeed)--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.

About NexMed

NexMed, Inc. is an emerging drug developer that is leveraging its proprietary drug technology to develop a significant pipeline of innovative pharmaceutical products to address significant unmet medical needs. The Company is also working with various pharmaceutical companies to explore the incorporation of NexACT into their existing drugs as a means of developing new patient-friendly transdermal products and extending patent lifespans and brand equity. For further information about the Company, go to

Statements under the Private Securities Litigation Reform Act: with the exception of the historical information contained in this release, the matters described herein contain forward-looking statements that involve risk and uncertainties that may individually or mutually impact the matters herein described, including but not limited to whether the FDA will accept the Company's NDA.

Source: NexMed

Issuer of this News Release is solely responsible for its content.
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