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

Is NDC 59148-0006-13 recalled?

Abilify · 30 TABLET in 1 BOTTLE, PLASTIC (59148-006-13)

Yes — this exact package was recalled

1 FDA recall names the code 59148-0006-13 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
Aripiprazole
Strength
ARIPIPRAZOLE 2 mg/1
Form
Tablet · Oral
Labeler
Otsuka America Pharmaceutical, Inc.
Type
Human Prescription Drug
Product code
59148-0006

Recalls naming this package

Class II ยท Moderate risk

ARIPiprazole Tablet

Labeling:Label Mixup; ARIPiprazole Tablet, 2 mg may be potentially mislabeled as tiZANidine HCl, Tablet, 2 mg, NDC 55111017915, Pedigree: AD21790_40, EXP: 5/1/2014; ATOMOXETINE HCL, Capsule, 80 mg, NDC 00002325030, Pedigree: AD30140_19, EXP: 5/7/2014; OLANZapine, Tablet, 7.5 mg, NDC 55111016530, Pedigree: AD46265_46, EXP: 5/15/2014; REPAGLINIDE, Tablet, 2 mg, NDC 00169008481, Pedigree: AD464

Terminated Labeling / mix-up Aidapak Services, LLC D-639-2014

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