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SafetyAlerts
April 30, 2003

Amerisource Health Services Has Recalled Premarin Tablets

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

PRODUCT
Premarin Tablets (Conjugated Estrogens Tablets, USP) 1.25 mg, 100 count bottles, Rx Only. Recall # D-229-3.

CODE
1D00076, Exp. 08/03.

RECALLING FIRM/MANUFACTURER
Recalled by: Amerisource Health Services, Corp., Columbus, OH, by recall notices on April 3, 2003.
Manufacturer: Ayerst Laboratories Inc., A Wyeth-Ayerst Company, Philadelphia, PA. Firm initiated recall is ongoing.

REASON
Dissolution failure (by manufacturer).

VOLUME OF PRODUCT IN COMMERCE
449 bottles of 100 tablets.

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.