Drug recall D-1042-2013
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.
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.
Lots and codes
Lot # L300192; Exp. 05/2017
Recall details
- Recalling firm
- Dr. Reddy's Laboratories, Inc., Bridgewater, NJ
- Quantity
- 18852 bottles
- Distribution
- Nationwide (& Puerto Rico)
- Type
- Voluntary: Firm initiated
- Recall initiated
- August 29, 2013
- Terminated
- March 20, 2014
Related products
- Ibu – drug information
- NDC 55111-682 Ibu · Ibuprofen 400 mg/1 · Dr. Reddy's Laboratories Limited
- NDC 55111-683 Ibu · Ibuprofen 600 mg/1 · Dr. Reddy's Laboratories Limited
- NDC 55111-684 Ibu · Ibuprofen 800 mg/1 · Dr. Reddy's Laboratories Limited