Over 2000 Posts MaryOld Posted January 18, 2002 Over 2000 Posts Report Share Posted January 18, 2002 Safetyalerts January 17, 2002 Rx Pak Has Recalled Premarin Tablets Memphis, TN (Safetyalerts) - The Food and Drug Administration (FDA) said that Rx Pak, Division of McKesson HBOC has recalled Premarin tablets, 1.25mg (Conjugated Estrogens Tablets, USP), Rx, 100 count tablets. PRODUCT Premarin tablets, 1.25mg (Conjugated Estrogens Tablets, USP), Rx, 100 count tablets, Recall # D-069-2. CODE Lot #03138, Exp 09/03, NDC# 00046-0866-81. RECALLING FIRM/MANUFACTURER Recalling Firm: Rx Pak, Division of McKesson HBOC Memphis, TN, by letter on 8/13/01. Manufacturer: Ayerst Laboratories, Rouses Point, NY. Firm initiated recall is ongoing. REASON Dissolution failure by manufacturer. VOLUME OF PRODUCT IN COMMERCE 41, 545 100 count bottles. DISTRIBUTION Nationwide. Quote Link to comment Share on other sites More sharing options...
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