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

Is NDC 0024-4142-60 recalled?

Multaq · 60 TABLET, FILM COATED in 1 BOTTLE (0024-4142-60)

Yes — this exact package was recalled

1 FDA recall names the code 0024-4142-60 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
Dronedarone
Strength
DRONEDARONE 400 mg/1
Form
Tablet, Film Coated · Oral
Labeler
Sanofi-Aventis U.S. LLC
Type
Human Prescription Drug
Product code
0024-4142

Recalls naming this package

Class II ยท Moderate risk

Dronedarone HCL

Labeling: Label Mixup: DRONEDARONE HCL, Tablet, 400 mg may be potentially as the following drug: METHYLERGONOVINE MALEATE, Tablet, 0.2 mg, NDC 43386014028, Pedigree: AD52778_40, EXP: 5/20/2014.

Terminated Labeling / mix-up Aidapak Services, LLC D-782-2014

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