Dr. Reddy's Laboratories, Inc. recalls IBU (TM) IBUPROFEN Tablets, USP, 800 mg, 500 -count bottle,(NDC 55111-684-05) Rx only, Distributed by Dr. Reddy's Labora

Recalled September 25, 2013 · FDA recall D-1042-2013 · Dr. Reddy's Laboratories

Hazard

Labeling: Incorrect or missing lot and/or exp date- This product is being recalled due to an incorrect expiration date of 05/2017. The correct expiration date is 10/2016. · FDA Class II

Units

18852 bottles

Sold at

Nationwide (& Puerto Rico)

Description

Labeling: Incorrect or missing lot and/or exp date- This product is being recalled due to an incorrect expiration date of 05/2017. The correct expiration date is 10/2016.

Product

IBU (TM) IBUPROFEN Tablets, USP, 800 mg, 500 -count bottle,(NDC 55111-684-05) Rx only, Distributed by Dr. Reddy's Laboratories, Inc., Bridgewater, NJ 08807 USA.

Manufacturer(s)

Dr. Reddy's Laboratories, Inc.

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →