Class II ยท Moderate risk
Fenofibrate
Labeling: Label Mixup: FENOFIBRATE, Tablet, 54 mg may have potentially been mislabeled as the following drug: FAMCICLOVIR, Tablet, 500 mg, NDC 00093811956, Pedigree: AD49448_4, EXP: 5/17/2014.
National Drug Code
Is NDC 0115-5511-10 recalled?
Fenofibrate · 90 TABLET in 1 BOTTLE (0115-5511-10)
Yes — this exact package was recalled
1 FDA recall names the code 0115-5511-10 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
- Fenofibrate
- Strength
- FENOFIBRATE 54 mg/1
- Form
- Tablet · Oral
- Labeler
- Amneal Pharmaceuticals of New York LLC
- Type
- Human Prescription Drug
- Product code
- 0115-5511
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
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