Product Detail

Product Description 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.

Recall Number D-1042-2013

Classification Class II

Code Info Lot # L300192; Exp. 05/2017

Product Distributed Qty 18852 bottles

Reason For Recall 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.

Event Detail

Event Id 66117

Product Type Drugs

Status Ongoing

Recalling Firm

Dr. Reddy's Laboratories, Inc.
City Bridgewater

State NJ
Country US

Voluntary / Mandated Voluntary: Firm Initiated

Recall Initiation Date 2013-08-29

Initial Firm Notification of Consignee or Public Letter

Distribution Pattern Nationwide (& Puerto Rico)