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November 30, 1999

SSS/Pfeiffer Pharmaceuticals Koleprin DM Caplets Recalled

Atlanta, GA (SafetyAlerts) - The Food and Drug Administration (FDA) today reported that SSS/Pfeiffer Pharmaceuticals is recalling Koleprin DM Caplets, cough and cold medication in 30 caplet bottles, because of friability failure at 3 month stability.

This ongoing Class III recall was initiated by the company, June 14, 1999 by letter.  This is the first notice the FDA has issued to the general public of the recall.

Over 2,500 units were distributed nationwide and bear the lot number and expiration date of #98603 EXP 2/01

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.