Pharmaceuticals, Inc. Recalls Lonox Tablets
August 17, 1999
Broomfield, CO (SafetyAlerts) - The Food and Drug
Administration (FDA) today reported that Geneva Pharmaceuticals, Inc. is recalling Lonox
Tablets because of subpotency.
Lonox Tablets (Diphenoxylate HCL, USP 2.5mg /
Atropine Sulfate, USP 0.025mg) in 100 and 1,000 tablet bottles, Rx combination ingredient
tablet for the management of diarrhea. NDC# 0781-1262-01 (100's) and 0781-1262-10
Lot #10057 EXP 09/01.
Geneva Pharmaceuticals, Inc., Broomfield, Colorado.
Manufacturer, by letter on August 2, 1999. Firm-initiated recall ongoing.
5,880,500 tablets were distributed.