FDA Drug · 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

Class III · Ongoing

Failed Tablet/Capsule Specifications

Affected lots / codes — check yours against thisLot #: C5406201, Exp 03/31/2028

Recalling firm: Dr. Reddy's Laboratories, Inc., Princeton, NJ
Classification: Class III (unlikely to cause harm)
Status: Ongoing
Quantity: 3416 botttles
Distribution: USA Nationwide
Recall initiated: October 29, 2024
Classified: November 15, 2024
Initiation: Voluntary: Firm initiated

Official source. This record is published by the U.S. FDA through the openFDA enforcement database. View the unmodified government record:
https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0047-2025%22

Important. Recalls target specific lots and codes — compare the affected lots above against your own product. This page reproduces public FDA data for readability; EveryRecall is independent and not affiliated with the FDA.

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