NDC 87441-006
Aripiprazole 5 mg tablet
On the label: Unit Dose Solutions, Inc.. It's repackaged: Unit Dose Solutions, Inc. rebottles it from Ajanta Pharma USA Inc.'s NDC 27241-052.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Ajanta Pharma Limited | Chhatrapati Sambhajinagar, India | Makes it | Problems found, fixed voluntarilyApr 21, 2026 · 6 inspections |
Repackaging site
- Unit Dose Solutions, Inc., Raleigh, NC, United States · repackages it
Recalls
- May 27, 2026 · Class II · Ajanta Pharma USA Inc
Product Mix-Up: A bottle containing Voriconazole Tablets 50 mg was labelled and distributed as Aripiprazole Tablets USP 30 mg.
Lots: Lot: PA00805, expires: 01/31/2029
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
- 5 mg
- Approval
- ANDA ANDA206174
- On the market since
- Jun 3, 2026
- Package NDCs
87441-006-01- Official label
- DailyMed (National Library of Medicine), updated Jun 3, 2026
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