FDAFDA · Food and drugs·Recall number D-0047-2025
IBU (ibuprofen) 600 mg tablets, 500-count bottle, Rx Only, Distributor: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540, Made in India, NDC 55111-683-05
Published November 27, 2024 · Recall initiated: October 29, 2024
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Failed Tablet/Capsule Specifications
What to do
Voluntary: Firm initiated
Recall details
- Brand
- IBU
- Manufacturer
- Dr. Reddy's Laboratories, Inc.
- Distributor
- USA Nationwide
- Lot
- Lot #: C5406201, Exp 03/31/2028
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
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