Akorn, Inc. Announces FDA Inspection Results

Business Wire, Dec 14, 2005

BUFFALO GROVE, Ill. -- Akorn, Inc. (AMEX:AKN) today announced the results from the latest FDA inspection of the Decatur, IL manufacturing facility. In correspondence received on December 13, 2005 from the Chicago District of the FDA, the FDA reported the satisfactory resolution of past cGMP issues and that the Decatur manufacturing facility is in compliance with current good manufacturing practice regulations. As a result of this inspection, Akorn is now eligible for new product approvals at the Decatur, IL manufacturing facility.

Arthur S. Przybyl, Akorn's President and Chief Executive Officer stated, "We are pleased to announce the results from the latest FDA inspection of our Decatur, IL manufacturing facility. Akorn remains committed to maintaining an adequate, comprehensive and robust quality system in order to remain in compliance with current good manufacturing practice regulations."

About Akorn, Inc.

Akorn, Inc. manufactures and markets sterile specialty pharmaceuticals. Akorn has manufacturing facilities located in Decatur, Illinois and Somerset, New Jersey and markets and distributes an extensive line of hospital and ophthalmic pharmaceuticals. Additional information is available at the Company's website at www.akorn.com.

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