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SafetyAlerts
October 10, 2002

Recall Update: Pharmaceutical Corp Allegra 60 mg Recall Complete

(SafetyAlerts) - The Food and Drug Administration (FDA) released the following information.

PRODUCT
Allegra 60 mg (Fexofenadine HCl Capsules), 14 and 60 count bottles, Rx only. Recall # D-001-3.

CODE
Lot no. 1044325, exp. 5/2004 and
Lot no. 1048818, exp. 10/2004.

RECALLING FIRM/MANUFACTURER
Recalling Firm: Pharmaceutical Corp. of America, Indianapolis, IN, by phone on September 10, 2002.
Manufacturer: Aventis Pharmaceuticals, Inc., Kansas City, MO. Firm initiated recall is complete.

REASON
Label mixup; bottles labeled as containing 60mg capsules actually contain 60mg tablets.

VOLUME OF PRODUCT IN COMMERCE
17 units.

DISTRIBUTION
CA and MI.

 
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During 2000 there were over
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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.