Lupin Pharmaceuticals Inc. recalls Suprax, Cefixime for Oral Suspension USP 500 mg/5 ml, 10mL (when reconstituted), Rx only, Manufactured for Lupin Pharmac
Recalled April 9, 2014 · FDA recall D-1186-2014 · 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
4,038 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, 10mL (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 27437-207-02.
Manufacturer(s)
Lupin Pharmaceuticals Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →