NDC 87441-019
Buspirone hydrochloride 15 mg tablet
On the label: Unit Dose Solutions, Inc.. It's repackaged: Unit Dose Solutions, Inc. rebottles it from Zydus Pharmaceuticals (USA) Inc.'s NDC 68382-182.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Zydus Lifesciences Limited | Ahmedabad, India | Makes it and tests it | Problems found, fixed voluntarilyAug 5, 2022 · 10 inspections, 3 with FDA action |
Repackaging site
- Unit Dose Solutions, Inc., Raleigh, NC, United States · repackages it
Product details
- Generic drug
- Buspirone: every company that makes it
- Form
- tablet, oral
- Strength
- 15 mg
- Approval
- ANDA ANDA078888
- On the market since
- Jun 15, 2026
- Package NDCs
87441-019-01- Official label
- DailyMed (National Library of Medicine), updated Jun 15, 2026
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