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

Is NDC 23155-0043-03 recalled?

leflunomide · 30 TABLET in 1 BOTTLE (23155-043-03)

Yes — this exact package was recalled

1 FDA recall names the code 23155-0043-03 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
leflunomide
Strength
LEFLUNOMIDE 10 mg/1
Form
Tablet · Oral
Labeler
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Type
Human Prescription Drug
Product code
23155-0043

Recalls naming this package

Class II ยท Moderate risk

LEFLUNOMIDE Tablet

Labeling: Label Mixup; LEFLUNOMIDE Tablet, 10 mg may be potentially mislabeled as DOXYCYCLINE HYCLATE, Capsule, 100 mg, NDC 00143314250, Pedigree: W002645, EXP: 6/5/2014; SEVELAMER CARBONATE, Tablet, 800 mg, NDC 58468013001, Pedigree: W002623, EXP: 6/4/2014.

Terminated Labeling / mix-up Aidapak Services, LLC D-527-2014

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