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.