Class III

Drug Recall: 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

Dr. Reddy's Laboratories, Inc. · October 29, 2024

Reason for Recall

Failed Tablet/Capsule Specifications

Distribution

USA Nationwide

States Affected

NATIONWIDE

Quantity Affected

3416 botttles

Source: FDA (openFDA Drug Enforcement)

Recall number: D-0047-2025

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.