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SafetyAlerts
April 2, 2003

IVAX Pharmaceuticals Has Recalled Terazosin Hydrochloride Capsules

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


PRODUCT
Terazosin Hydrochloride Capsules, 1 mg, 500 count bottles, Rx only. Recall # D-191-3.

CODE
Lot number 4336-707 Exp. Date Jun 03.

RECALLING FIRM/MANUFACTURER
Recalling Firm: IVAX Pharmaceuticals, Miami, FL, by letters on February 11, 2003.
Manufacturer: Zenith Goldline Pharmaceuticals, Inc. Firm initiated recall is ongoing.

REASON
Dissolution Failure; 18 month timepoint (stability).

VOLUME OF PRODUCT IN COMMERCE
50 bottles.

DISTRIBUTION
Nationwide.

 

 
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Health Professional:

Did you know?
During 2000 there were over
1050 products recalled in the United
States for safety reasons!

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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.