NDC 67046-1352
Buspirone hydrochloride 7.5 mg tablet
On the label: Coupler LLC. It's repackaged: Coupler LLC rebottles it from Zydus Pharmaceuticals (USA) Inc.'s NDC 68382-623.
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
- Coupler LLC, West Chester, PA, United States · repackages it
Product details
- Generic drug
- Buspirone: every company that makes it
- Form
- tablet, oral
- Strength
- 7.5 mg
- Approval
- ANDA ANDA078888
- On the market since
- Jun 10, 2026
- Package NDCs
67046-1352-3- Official label
- DailyMed (National Library of Medicine), updated Jun 10, 2026
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