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SafetyAlerts
August 6, 2003

Solvay Pharmaceuticals Has Recalled LITHOBID Tablets

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

PRODUCT
LITHOBID Tablets (Lithium Carbonate, USP) Slow Release Tablets, 300 mg, 100 tablet bottles, Rx only. Recall # D-286-3.

CODE
Lot 92263.

RECALLING FIRM/MANUFACTURER
Solvay Pharmaceuticals, Inc., Marietta, GA, by letter on June 20, 2003. Firm initiated recall is ongoing.

REASON
Dissolution failure; 12 month stability.

VOLUME OF PRODUCT IN COMMERCE
14,029 bottles of 100 tablets.

DISTRIBUTION
Nationwide
.

 
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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.