drugs Class II Updated 2013-09-25

Dr. Reddy's Laboratories, Inc. recalls IBU (TM) IBUPROFEN Tablets, USP, 800 mg, 500 -count bottle,(

Recalled 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.

Hazard / Issue

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.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Lot # L300192; Exp. 05/2017
View official government recall

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