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SafetyAlerts
July 23, 2003

Amerisource Health Services Has Recalled Premarin

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

PRODUCT
Premarin 0.625 mg Tablets, U.D. 100's (conjugated estrogens tablets, USP) Rx only. Recall # D-267-3.

CODE
Lot Number IJ00170.

RECALLING FIRM/MANUFACTURER
Amerisource Health Services Corp., Columbus, OH, by letters on June 2, 2003. Firm initiated recall is ongoing.

REASON
Dissolution failure (by manufacturer Wyeth)

VOLUME OF PRODUCT IN COMMERCE
5 cartons - 100 unit dose tablets.

DISTRIBUTION
Nationwide
.

 
Selected Recent Recalls


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.