Lupin Pharmaceuticals Inc. recalls Suprax, Cefixime for Oral Suspension USP, 500 mg/5 ml, 20 mL (when reconstituted), Rx only, Manufactured for Lupin Phar
Recalled April 9, 2014 · FDA recall D-1187-2014 · Lupin Pharmaceuticals
Hazard
Failed Impurities/Degradation Specifications: Product did not meet specification in total impurities at the 9-month stability station. · FDA Class III
Units
5,172 bottles
Sold at
Nationwide
Description
Failed Impurities/Degradation Specifications: Product did not meet specification in total impurities at the 9-month stability station.
Product
Suprax, Cefixime for Oral Suspension USP, 500 mg/5 ml, 20 mL (when reconstituted), Rx only, Manufactured for Lupin Pharmaceuticals, Inc. 111 South Calvert Street, Baltimore, MD 21202, Manufactured by Lupin Limited Mumbai 400 058 India, NDC 27437-207-03.
Manufacturer(s)
Lupin Pharmaceuticals Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →