August 6, 2003
McKesson Has Recalled Premarin Tablets
The Food and Drug Administration (FDA) released the following information.
Premarin Tablets, (Conjugated Estrogens Tablets, USP), 0.625 mg, 100 tablet
bottles, Rx Only. Recall # D-295-3.
03831 Exp 4/04.
Recalling Firm: McKesson, Memphis, TN, by letters on May 20, 2003.
Manufacturer: Ayerst Laboratories, Inc., A Wyeth-Ayerst Company,
Philadelphia, PA. Firm initiated recall is ongoing.
Dissolution Failure by the manufacturer (Wyeth).
VOLUME OF PRODUCT IN COMMERCE