FDAFDA · Food and drugs·Recall number D-0290-2021
Famotidine Tablets USP 40mg, 1,000-count bottles, Rx only, Distributed by: Aurobindo Pharma USA, Inc. 279 Princeton-Hightstown Road East Windsor, NJ 08520 Made in India, NDC 65862-860-99
Published March 10, 2021 · Recall initiated: January 20, 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
Presence of foreign tablets/capsules: Famotidine 20mg and ibuprofen 400mg tablets were found in a lot of famotidine 40mg.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- FAMOTIDINE
- Manufacturer
- Aurobindo Pharma USA Inc.
- Distributor
- TX, CA, GA, PA
- Lot
- Lot #: P2000467, Exp 7/2022
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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