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November 30, 1999

Hoechst Marion Roussel, Inc. Anzemet Tablets Recalled

Cincinnati, OH (SafetyAlerts) - The Food and Drug Administration (FDA) today reported that Hoechst Marion Roussel, Inc. is recalling Anzemet Tablets because stability (6 month) test failure elevated degradation the product.

The Anzemet Tablets (Dolasetron Mesylate) recalled are 100 mg, bottles of 5 tablets used anti-nauseant and anti-emetic and have the NDC #0088-1203-05.

This ongoing  Class III recall was initiated by the company, October 5, 1999 by letter.  This is the first notice the FDA has issued to the general public of the recall.

Over 10,000 bottles were distributed in Ohio and Missouri and bear the lot numbers and expiration dates of:
3001616 EXP 2/01
3003145 EXP 2/01
3003148 EXP 4/01

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.