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FDAFDA · Food and drugs·Recall number D-0229-2022

Cefixime Capsules 400 mg, 50 capsules bottles, Rx Only, Manufactured by: Alken Laboratories Ltd., Mumbai - 400 013, India, Distributed by: Ascend Laboratories LLC, Parsippany, NJ, 07054 NDC 67877-584-50

Published November 17, 2021 · Recall initiated: November 3, 2021

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

What to do

Voluntary: Firm initiated · Letter

Recall details

Brand
CEFIXIME
Manufacturer
Ascend Laboratories LLC
Distributor
Nationwide
Lot
Lot 20140282, exp Dec 2021
Risk classification
Class II
Area (FDA)
drug
Country
United States

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