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Glucophage XR tablets Recall

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One of the members sent this to me.

Eunice

Bristol-Myers Squibb Company Has Recalled Glucophage

XR tablets

Reason: Subpotency; some tablets may contain less than

the minimum

specification for potency (blend validation).

Distribution: Nationwide.

http://www.safetyalerts.com/recall/f/02.2/f0003170.htm

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HREF= " http://www.safetyalerts.com/recall/f/02.2/f0003170.htm " >

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