Class III · Low risk
Abilify (aripiprazole)
Cross Contamination with Other Products
National Drug Code
Is NDC 59148-0011-35 recalled?
Abilify · 100 TABLET in 1 BLISTER PACK (59148-011-35)
Yes — this exact package was recalled
1 FDA recall names the code 59148-0011-35 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 30 mg/1
- Form
- Tablet · Oral
- Labeler
- Otsuka America Pharmaceutical, Inc.
- Type
- Human Prescription Drug
- Product code
- 59148-0011
Recalls naming this package
Class II · Moderate risk
ABILIFY (aripiprazole)
CGMP Deviations: A drum of Abilify 30 mg Tablets rejected during the compression stage was not segregated from the other portion of the lot and was inadvertently shipped, packaged and distributed.
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
- 59148-0009 Abilify 2
- 59148-0006 Abilify 1
- 59148-0007 Abilify 1
- 59148-0008 Abilify 1
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