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Safety Alerts
August 17, 1999

Geneva Pharmaceuticals, Inc. Recalls Lonox Tablets

Broomfield, CO (SafetyAlerts) - The Food and Drug Administration (FDA) today reported that Geneva Pharmaceuticals, Inc. is recalling Lonox Tablets because of subpotency.

PRODUCT
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 (1000's).

Recall #D-303-9.

CODE
Lot #10057 EXP 09/01.

MANUFACTURER
Geneva Pharmaceuticals, Inc., Broomfield, Colorado.

RECALLED BY
Manufacturer, by letter on August 2, 1999. Firm-initiated recall ongoing.

DISTRIBUTION
Nationwide.

QUANTITY
5,880,500 tablets were distributed.

 

The information contained herein has been obtained from sources that the Company believes to be reliable, however, the Company has not independently verified or confirmed the information and the recipient acknowledges that no representations or warranties are being made in connection with the use of the information.