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Eisai Inc. announced that the U. Food and Drug Administration has accepted for review the New Drug Application (NDA) for the Aricept(R) atch., a subsidiary of Teikoku Seiyaku Co.

, and Eisai are seeking approval of the weekly Aricept atch in the treatment of mild, moderate and severe stages of Alzheimer's disease.

Teikoku Seiyaku and Eisai Co. Ltd. announced in early 2009 that the companies signed agreements regarding the development and marketing of the Aricept atch in Japan, the U., Eisai Inc. will hold marketing rights in the U.

S. and will Prozac land audiobook the Aricept atch with fizer. The acceptance of the NDA indicates that the FDA deems the company's submission to be sufficiently complete to review. The NDA was submitted to the FDA on June 30, 2010.

The Aricept atch is a weekly transdermal patch that was developed to provide an alternative formulation for Alzheimer's patients. Eisai has a long-standing commitment to the Alzheimer's disease community and is dedicated to providing new treatment options. Market data is Phenaphen cod 2 strength at least 15 minutes.

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