Class III · Low risk
Abilify (aripiprazole)
Cross Contamination with Other Products
National Drug Code
Is NDC 59148-0009-13 recalled?
Abilify · 30 TABLET in 1 BOTTLE, PLASTIC (59148-009-13)
Yes — this exact package was recalled
2 FDA recalls name the code 59148-0009-13 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.
1 of these recalls is still ongoing.
- Active ingredient
- Aripiprazole
- Strength
- ARIPIPRAZOLE 15 mg/1
- Form
- Tablet · Oral
- Labeler
- Otsuka America Pharmaceutical, Inc.
- Type
- Human Prescription Drug
- Product code
- 59148-0009
Recalls naming this package
Class II · Moderate risk
ARIPiprazole Tablet
Labeling:Label Mixup; ARIPiprazole, Tablet, 15 mg may be potentially mislabeled as ATOMOXETINE HCL, Capsule, 40 mg, NDC 00002322930, Pedigree: AD21790_82, EXP: 5/1/2014; PRAMIPEXOLE DI-HCL, Tablet, 0.125 mg, NDC 13668009190, Pedigree: AD25264_10, EXP: 5/3/2014.
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
- 59148-0011 Abilify 2
- 59148-0006 Abilify 1
- 59148-0007 Abilify 1
- 59148-0008 Abilify 1
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