Class II ยท Moderate risk
Ibuprofen Tablets
CGMP Deviations: Various strengths of ibuprofen tablets/caplets are being recalled due to complaints of odor related to CGMP deficiencies.
National Drug Code
Is NDC 25000-0123-27 recalled?
Ibuprofen
Yes — this exact package was recalled
1 FDA recall names the code 25000-0123-27 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.
- Active ingredient
- Ibuprofen
- Strength
- IBUPROFEN 800 mg/1
- Form
- Tablet · Oral
- Labeler
- Marksans Pharma Limited
- Type
- Human Prescription Drug
- Product code
- 25000-0123
Recalls naming this package
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
- 25000-0114 Ibuprofen 1
- 25000-0117 Ibuprofen 1
- 25000-0121 Ibuprofen 1
- 25000-0122 Ibuprofen 1
- 25000-0136 Ibuprofen 1
Free recall alerts
Know the day your medication is recalled
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