NDC 62332-101

Aripiprazole 20 mg tablet

On the label: Alembic Pharmaceuticals Inc..

Where it's made

Recalls

• Jun 10, 2020 · Class II · Alembic Pharmaceuticals Limited
  Labeling: Label mix up: Bottles labeled as aripiprazole 2 mg, 30 count had aripiprazole 5 mg tablets, 100 count.
  Lots: Lot: 1905003298 Exp. 01/31/2021

Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.

Product details

Generic drug

Aripiprazole: every company that makes it

Form

tablet, oral

Strength

20 mg

Approval

ANDA ANDA202101

On the market since

Jul 7, 2016

Package NDCs

62332-101-10 62332-101-30 62332-101-31 62332-101-71 62332-101-91

Official label

DailyMed (National Library of Medicine), updated Jun 25, 2025

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