US Drug Recall Register
Class III · Low risk Terminated Initiated Jan 31, 2013 (14 years ago)

Suprax (cefixime for oral suspension) USP, 100 mg/5 mL, 50 mL bottles (when…

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Discoloration; Product may not meet specifications for color description once reconstituted.

What was recalled

Suprax (cefixime for oral suspension) USP, 100 mg/5 mL, 50 mL bottles (when reconstituted), Manufactured for Lupin Pharmaceuticals, Inc. 111 South Calvert Street, Baltimore, MD 21202, Manufactured by Lupin Limited Mumbai 400 058 India, NDC 68180-202-03.

Recalling firm
Lupin Pharmaceuticals Inc.
NDC code
68180-202-03
Origin
MD, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-264-2013

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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