Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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National Drug Code

Is NDC 64764-0918-30 recalled?

Uloric · 30 TABLET in 1 BOTTLE (64764-918-30)

Yes — this exact package was recalled

1 FDA recall names the code 64764-0918-30 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
febuxostat
Strength
FEBUXOSTAT 40 mg/1
Form
Tablet · Oral
Labeler
Takeda Pharmaceuticals America, Inc.
Type
Human Prescription Drug
Product code
64764-0918

Recalls naming this package

Class II ยท Moderate risk

FEBUXOSTAT Tablet

Labeling: Label Mixup; FEBUXOSTAT Tablet, 40 mg may be potentially mislabeled as methylPREDNISolone, Tablet, 4 mg, NDC 59746000103, Pedigree: AD21811_17, EXP: 5/1/2014; tiZANidine HCl, Tablet, 2 mg, NDC 55111017915, Pedigree: W002663, EXP: 6/5/2014; SODIUM CHLORIDE, Tablet, 1000 mg, NDC 00527111610, Pedigree: W003926, EXP: 7/1/2014.

Terminated Labeling / mix-up Aidapak Services, LLC D-698-2014

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