LLC Recalls Yodoxin 650 mg Tablets
August 4, 1999
Piscataway, NJ (SafetyAlerts) - The Food and Drug
Administration (FDA) today reported that Glenwood, LLC is recalling Yodoxin 650 mg Tablets
because of subpotency (6 month stability).
Yodoxin 650 mg Tablets (lodoquinol USP), in 100
tablet bottles, Rx anti-amebic. NDC #0516-0093-01.
Lot #49835 EXP 9/2001.
Glenwood, LLC, Piscataway, New Jersey.
Manufacturer, by letter on February 22, 1999. Firm-initiated recall ongoing.
976 bottles were distributed.