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Class II · ModerateRecall completed

Cefixime

Could cause temporary or reversible harm; serious harm is unlikely.

Does this affect you?
Check your lot numberLot #: F304833, Exp 06/2025
Where it was soldNationwide in the USA
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.

What happened

Failed Impurities/Degradation Specifications

What to do

  1. Check the lot number and expiry on your medicine against the recall above.
  2. Talk to your pharmacist or doctor before changing anything — don't stop on your own.
  3. Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).

Who makes it

Made byLupin Limited, Mandideep 462 046 INDIA foreign manufacturer
Brand nameCEFIXIME
Generic nameCEFIXIME
Active ingredient(s)CEFIXIME
Distributed by / forLupin Pharmaceuticals, Inc., Baltimore, Maryland 21202
NDC68180-405-01
Show the full FDA record
Full product labelCefixime for Oral Suspension 100mg/5mL, 50 mL bottle, Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc., Baltimore, Maryland 21202, Manufactured by:Lupin Limited, Mandideep 462 046 INDIA, NDC 68180-405-01
Recalling firmLupin Pharmaceuticals Inc.
DistributionNationwide in the USA
Quantity4,608 Bottles
Recall initiated2024-01-03
Report date2024-02-07
Recall completed2024-12-27
Recall numberD-0274-2024
ClassificationClass II
FDA statusTerminated
Origin on fileBaltimore MD United States

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Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗

This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.