FDAJune 5, 2017drug
EliquisTablets 5mg, 60 count bottle, Rx Only, Marketed by: Bristol-Meyers Squibb Company Princeton, NJ 08543 USA and Pfizer Inc. New York, NY 10017 USA, NDC 0003-0894-21
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
Labeling: Label Mix-up: One bottle of Eliquis 5 mg tablet was found to contain lower-strength Eliquis 2.5 mg tablets only instead of the labeled 5 mg tablets.
What to do
FDA enforcement status: Terminated
Brands named
bristol myers squibbbristolbristol myers
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
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