Safety Alerts Saves Lives
Safety Alerts  
 
Home Privacy About Us Contact Us Change Preferences

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
.

 
Selected Recent Recalls


Health Professional:

Did you know?
During 2000 there were over
1050 products recalled in the United
States for safety reasons!

How many did you hear about?

Sign-up for SafetyAlerts by Email -
The free internet newsletter that could
some day literally save your life - or
the life of someone you know.

 

The information contained herein has been obtained from sources that the Company believes to be reliable, however, the Company has not independently verified or confirmed the information and the recipient acknowledges that no representations or warranties are being made in connection with the use of the information.