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The Female Health Company Announces FDA Acceptance for Review of Its FC2 Premarket Approval Application
Date:2/6/2008

CHICAGO, Feb. 6 /PRNewswire-FirstCall/ -- The Female Health Company (Amex: FHC) today announced that the Food and Drug Administration (FDA) has determined that the Premarket Approval Application (PMA) it submitted for its second generation product, FC2 female condom, has been accepted for review. The Center for Devices and Radiological Health (CDRH) received FHC's PMA on January 8, 2008.

About The Female Health Company, Inc.

The Female Health Company, based in Chicago, Illinois, manufactures and markets the FC Female Condom(R), which is primarily distributed by public health organizations and donor groups in over 90 developing countries around the world. World-wide, the Female Condom is available in various programs in 108 countries. The Company owns certain worldwide rights to the FC Female Condom(R), including patents that have been issued in the United States, United Kingdom, Japan, France, Italy, Germany, Spain, the European Patent Convention, the People's Republic of China, Canada, South Korea and Australia. FC Female Condom(R) is the only available FDA-approved product controlled by a woman that offers dual protection against sexually transmitted diseases, including HIV/AIDS, and unintended pregnancy.

"Safe Harbor" statement under the Private Securities Litigation Reform Action of 1995: The statements in this release which are not historical fact are forward-looking statements based upon the Company's current plans and strategies, and reflect the Company's current assessment of the risks and uncertainties related to its business, including such things as product demand and market acceptance; the economic and business environment and the impact of government pressures; currency risks; capacity; efficiency and supp
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SOURCE The Female Health Company
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