June 25, 2003
Purdue Frederick Has Recalled
The Food and Drug Administration (FDA) has released the following
OxyContin Tablets (oxycodone hydrochloride controlled-release), 10 mg, 25
count unit dose packages, Rx only, For Hospital Use. Recall # D-265-3.
Lot SG11 exp. 2/28/2006.
The Purdue Frederick Company, Stamford, CT, by telephone on March 17, and
21, 2003. Firm initiated recall is ongoing.
NDA Filing Discrepancy; supplement not filed for new supplier of inactive
VOLUME OF PRODUCT IN COMMERCE
9,732-25 count blister packs.