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.
Reported: September 25, 2013 Initiated: August 29, 2013 #D-1042-2013
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.
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.
Details
- Recalling Firm
- Dr. Reddy's Laboratories, Inc.
- Units Affected
- 18852 bottles
- Distribution
- Nationwide (& Puerto Rico)
- Location
- Bridgewater, NJ
Frequently Asked Questions
What product was recalled? ▼
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.. Recalled by Dr. Reddy's Laboratories, Inc.. Units affected: 18852 bottles.
Why was this product recalled? ▼
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.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on September 25, 2013. Severity: Moderate. Recall number: D-1042-2013.
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