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More Counterfeit Lipitor Lots Identified
Since learning of problems with this product late last month, FDA investigators have aggressively pursued a variety of leads all along the supply and distribution chain. Evidence of the new lots of implicated Lipitor arose in the context of FDA’s investigation.
FDA’s advice to healthcare providers and consumers remains the same as when the agency issued its original alert on counterfeit Lipitor May 23, 2003. They should check the packaging very carefully before using Lipitor. Patients who have any of the product (labeled as “Repackaged by: MED-PRO, INC. Lexington, NE 68850”) with any of the following lot numbers should not take it, and they should return the product to their pharmacies:
20722V – 90-tablet bottles, 10 mg., Expiration 09-2004
04132V – 90-tablet bottles, 10 mg., Expiration 01-2004
16942V – 90-tablet bottles, 10 mg., Expiration 09-2004
20842V – 90-tablet bottles, 10 mg., Expiration 09-2004
16092V – 90-tablet bottles, 10 mg., Expiration 07-2004
D270481 – 90 tablet bottles, 20 mg.,Expiration not available.
FDA is working closely with the individual states and with health professionals, especially with pharmacists and pharmacy associations, to alert them to this counterfeit product. Many patients taking Lipitor do not receive it in the 90-tablet bottles being recalled, but in smaller quantities from their pharmacists. Patients who are not sure whether they have the implicated product should check with their pharmacist.
FDA is also working closely with the manufacturer of Lipitor, Pfizer, Inc., on this counterfeiting problem. FDA supports the activities of legitimate manufacturers to inform the public about counterfeit products and how to identify them. Last month, FDA entered into an agreement with a major pharmaceutical trade association to cooperate more closely on cases of suspected counterfeit products.
FDA’s investigation into this matter is continuing.