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Safety Alerts
August 17, 1999

RIJ Pharmaceutical Recalls Losopan Antacid

Middletown, NY (SafetyAlerts) - The Food and Drug Administration (FDA) today reported that RIJ Pharmaceutical Corporation is recalling Losopan Antacid because of mislabeling.  Some bottles bear an incorrect antacid back label (Goldline Genaton).

PRODUCT
Losopan Antacid (Magaldrate Oral Suspension Antacid 540 mg/5mL, in 12 fluid ounce bottles, OTC indicated for the relief of heartburn, sour stomach and/or acid indigestion and upset stomach associated with these symptoms.NDC #0182-6078-39.

Recall #D-302-9.

CODE
Lot #81235 EXP 12/00.

MANUFACTURER
RIJ Pharmaceutical Corporation, Middletown, New York.

RECALLED BY
Manufacturer, by letter and fax dated July 21, 1999. Firm-initiated recall ongoing.

DISTRIBUTION
Kentucky.

QUANTITY
5,208 bottles 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.