April 30, 2003
Amerisource Health Services Has
Recalled Premarin Tablets
The Food and Drug
Administration (FDA) released the following information.
Premarin Tablets (Conjugated Estrogens Tablets, USP) 1.25 mg, 100 count
bottles, Rx Only. Recall # D-229-3.
1D00076, Exp. 08/03.
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.
Dissolution failure (by manufacturer).
VOLUME OF PRODUCT IN COMMERCE
449 bottles of 100 tablets.