Dr. Reddy's Laboratories, Inc. recalls IBU (ibuprofen) 600 mg tablets, 500-count bottle, Rx Only, Distributor: Dr. Reddy's Laboratories Inc., Princeton, NJ 08
Recalled November 27, 2024 · FDA recall D-0047-2025 · Dr. Reddy's Laboratories
Hazard
Failed Tablet/Capsule Specifications · FDA Class III
Units
3416 botttles
Sold at
USA Nationwide
Description
Failed Tablet/Capsule Specifications
Product
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
Manufacturer(s)
Dr. Reddy's Laboratories, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →