January 17, 2002Rx Pak Has Recalled Premarin Tablets
Memphis, TN (SafetyAlerts)
- The Food and Drug Administration (FDA) said that Rx Pak, Division of
McKesson HBOC has recalled
1.25mg (Conjugated Estrogens Tablets, USP), Rx, 100 count tablets.
Premarin tablets, 1.25mg (Conjugated Estrogens Tablets, USP), Rx, 100 count
tablets, Recall # D-069-2.
Lot #03138, Exp 09/03, NDC# 00046-0866-81.
Recalling Firm: Rx Pak, Division of McKesson HBOC Memphis, TN, by letter on
Manufacturer: Ayerst Laboratories, Rouses Point, NY.
Firm initiated recall is ongoing.
Dissolution failure by manufacturer.
VOLUME OF PRODUCT IN COMMERCE
41, 545 100 count bottles.