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FDAFDA · Food and drugs·Recall number D-0841-2016

Ondansetron Tablets USP, 4 mg, 30 count bottles, Rx only, Manufactured by: Dr. Reddy's Laboratories, Bachupally, India --- NDC 56111-153-30

Published May 18, 2016 · Recall initiated: March 30, 2016

Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.

What's the hazard

Failed Impurities/Degradation Specifications; 12 month stability time point

What to do

Voluntary: Firm initiated · Letter

Recall details

Manufacturer
Dr. Reddy's Laboratories, Inc.
Distributor
Nationwide
Lot
Lot number C500691, exp 12/2016
Risk classification
Class II
Area (FDA)
drug
Country
United States

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