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Class III · Lower riskRecall completed

Amoxicillin

Unlikely to cause harm — often a labeling or packaging issue.

Does this affect you?
Check your lot numberLot #: AS1466A, Exp. Jan 2019
Where it was soldNationwide
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

Labeling: Label Error on Declared Strength: Some bottles miss a color coded panel where the strength of the product is typically displayed.

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 byHikma Pharmaceuticals, P.O. Box 183400, Amman 11118 - Jordan
Brand nameAMOXICILLIN
Generic nameAMOXICILLIN
Active ingredient(s)AMOXICILLIN
Distributed by / forWest-Ward Pharmaceuticals Corp.
NDC0143-9887-01
Show the full FDA record
Full product labelAmoxicillin for Oral suspension, USP 400 mg/5 mL, 100 mL (when reconstituted), Rx only, Manufactured by: Hikma Pharmaceuticals, P.O. Box 183400, Amman 11118 - Jordan, NDC 0143-9887-01
Recalling firmWest-Ward Pharmaceuticals Corp.
DistributionNationwide
Quantity32,102 bottles
Recall initiated2016-11-04
Report date2016-11-30
Recall completed2017-06-16
Recall numberD-0147-2017
ClassificationClass III
FDA statusTerminated
Origin on fileEatontown NJ United States

Related

Amoxicillin recallsRecent drug recallsCheck another medication

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.