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SafetyAlerts
May 21, 2003

Teva Pharmaceuticals Has Recalled Enalapril Maleate Tablets

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

PRODUCT
Enalapril Maleate Tablets, USP, 10 mg, bottles of 1000, TEVA, Rx only. Recall # D-247-3.

CODE
Lot # 15741 exp 5/31/03.

RECALLING FIRM/MANUFACTURER
Teva Pharmaceuticals USA, North Wales, PA, by letters dated March 19, 2003. Firm initiated recall is
ongoing.

REASON
Degradation: Related compound specification failure (18 month stability).

VOLUME OF PRODUCT IN COMMERCE
1,182 bottles.

DISTRIBUTION
Nationwide.

 
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Health Professional:

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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.