FDA-Drug2013-09-25Class II
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.
Dr. Reddy's Laboratories, Inc.
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.
Sold states
Nationwide (& Puerto Rico)
Affected count
18852 bottles
Manufactured in
200 Somerset Corporate Blvd Fl 7th, N/A, Bridgewater, NJ, United States
Products
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.
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1042-2013Don't want to check this manually?
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