Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
RxRecalls Get alerts

National Drug Code

Is NDC 24338-0122-13 recalled?

Ery-Tab · 100 TABLET, DELAYED RELEASE in 1 BOTTLE (24338-122-13)

Yes — this exact package was recalled

1 FDA recall names the code 24338-0122-13 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
Erythromycin
Strength
ERYTHROMYCIN 250 mg/1
Form
Tablet, Delayed Release · Oral
Labeler
Arbor Pharmaceuticals, Inc.
Type
Human Prescription Drug
Product code
24338-0122

Recalls naming this package

Class II ยท Moderate risk

ERYTHROMYCIN DR EC Tablet

Labeling: Label Mixup; ERYTHROMYCIN DR EC Tablet, 250 mg may be potentially mislabeled as methylPREDNISolone, Tablet, 4 mg, NDC 00781502201, Pedigree: AD46426_10, EXP: 5/15/2014.

Terminated Labeling / mix-up Aidapak Services, LLC D-536-2014

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