NDC 70518-2281
Aripiprazole 10 mg tablet
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Alembic Pharmaceuticals Inc.'s NDC 62332-099.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Alembic Pharmaceuticals Limited | Panchmahal, India | Makes it | No problems foundJul 26, 2024 · 8 inspections |
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
- 10 mg
- Approval
- ANDA ANDA202101
- On the market since
- Aug 26, 2019
- Package NDCs
70518-2281-070518-2281-170518-2281-2- Official label
- DailyMed (National Library of Medicine), updated Jul 22, 2026
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