October 4, 2000Suprax Tablets Recalled
public notice issued by FDA of 'completed recall'...
IN (SafetyAlerts) - The Food and
Drug Administration (FDA) said today that Pharmaceutical Corporation of America is
recalling certain Suprax Tablets because of a label mix-up. The Suprax Tablets bore
a bar code for Cefadroxil.
This is the first public notice of
this Class II
recall issued by FDA.
Suprax Tablets, 400 mg, Rx, used to treat bacterial infections. NDC
Lot #S078RB EXP 1/31/00.
Pharmaceutical Corporation of America, Carmel, Indiana.
Manufacturer, by telephone on May 11, 2000. Firm-initiated recall **complete.
**Completed recall: While the FDA has completed
processing of this particular recall, it does not mean this particular product has been
fully accounted for.
56 bottles were distributed.
Questions concerning this recall may be directed
to the FDA at 1-888-INFO-FDA.
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