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 53943-0291-12 recalled?
Ibuprofen · 1 BOTTLE, PLASTIC in 1 CARTON (53943-291-12) / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Yes — this exact package was recalled
1 FDA recall names the code 53943-0291-12 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 200 mg/1
- Form
- Tablet, Film Coated · Oral
- Labeler
- Discount Drug Mart
- Type
- Human OTC Drug
- Product code
- 53943-0291
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
- 53943-0021 See recall 1
- 53943-0107 Multi Symptom Antacid 1
- 53943-0123 Loperamide Hydrochloride 1
- 53943-0192 See recall 1
- 53943-0292 Ibuprofen 1
- 53943-0871 See recall 1
Free recall alerts
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