Class III · Lower riskActive recall
Ibu
Unlikely to cause harm — often a labeling or packaging issue.
Does this affect you?
Check your lot numberLot #: C5406201, Exp 03/31/2028
Where it was soldUSA Nationwide
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.
What happened
Failed Tablet/Capsule Specifications
What to do
- Check the lot number and expiry on your medicine against the recall above.
- Talk to your pharmacist or doctor before changing anything — don't stop on your own.
- Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).
Who makes it
Made byMade in India foreign manufacturer
| Brand name | IBU |
| Generic name | IBUPROFEN |
| Active ingredient(s) | IBUPROFEN |
| Distributed by / for | Dr. Reddy's Laboratories, Inc. |
| NDC | 55111-683-05 |
Show the full FDA record
| Full product label | IBU (ibuprofen) 600 mg tablets, 500-count bottle, Rx Only, Distributor: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540, Made in India, NDC 55111-683-05 |
| Recalling firm | Dr. Reddy's Laboratories, Inc. |
| Distribution | USA Nationwide |
| Quantity | 3416 botttles |
| Recall initiated | 2024-10-29 |
| Report date | 2024-11-27 |
| Recall completed | — |
| Recall number | D-0047-2025 |
| Classification | Class III |
| FDA status | Ongoing |
| Origin on file | Princeton NJ United States |
Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗
This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.