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November 30, 1999

Mikart, Inc. Duratuss G Tablets Recalled

Atlanta, GA (SafetyAlerts) - The Food and Drug Administration (FDA) today reported that Mikart, Inc. is recalling Duratuss G Tablets because of dissolution failure.

This ongoing Class III recall was initiated by the company, June 22, 1999 by telephone.  This is the first notice the FDA has issued to the general public of the recall.

The recalled tablets were distributed in Wisconsin and bear the lot numbers of J980726A or J9800727A.

Questions concerning this recall may be directed to the FDA at 1-888-INFO-FDA.

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The information contained herein has been obtained from sources that the Company believes to be reliable, however, the Company has not independently verified or confirmed the information and the recipient acknowledges that no representations or warranties are being made in connection with the use of the information.