Class III · Low risk
IBU (ibuprofen)
Failed Tablet/Capsule Specifications
National Drug Code
Is NDC 55111-0683-01 recalled?
Ibu · 100 TABLET in 1 BOTTLE (55111-683-01)
Yes — this exact package was recalled
1 FDA recall names the code 55111-0683-01 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
2 of these recalls are still ongoing.
- Active ingredient
- Ibuprofen
- Strength
- IBUPROFEN 600 mg/1
- Form
- Tablet · Oral
- Labeler
- Dr. Reddy's Laboratories Limited
- Type
- Human Prescription Drug
- Product code
- 55111-0683
Recalls naming this package
Class II · Moderate risk
IBU Ibuprofen Tablets
Failed impurities/degradation specifications: results for unknown impurity, were 0.13% and 0.11% respectively, exceeding the 0.10% specification limit.
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Other recalled products from this labeler
- 55111-0121 Atorvastatin Calcium 4
- 55111-0123 Atorvastatin Calcium 4
- 55111-0180 Tizanidine 4
- 55111-0136 Zenatane 3
- 55111-0179 Tizanidine 3
- 55111-0320 Glimepiride 3
Free recall alerts
Know the day your medication is recalled
Tell us what you take. When FDA posts a recall announcement or classifies a recall for one of your medications, we email you in plain English, with what to check. No account needed.