NDC 80425-0334
Buspirone Hydrochloride 5 mg tablet
On the label: Advanced Rx Pharmacy of Tennessee, LLC. It's repackaged: Advanced Rx Pharmacy of Tennessee, LLC rebottles it from Aurobindo Pharma Limited's NDC 59651-389.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Apl Healthcare Limited | Tirupati, India | Makes it and tests it | Problems found, fixed voluntarilyDec 17, 2025 · 5 inspections |
Repackaging site
- Advanced Rx Pharmacy of Tennessee, LLC, Nashville, TN, United States · repackages it
Product details
- Generic drug
- Buspirone: every company that makes it
- Form
- tablet, oral
- Strength
- 5 mg
- Approval
- ANDA ANDA078246
- On the market since
- May 19, 2023
- Package NDCs
80425-0334-180425-0334-280425-0334-3- Official label
- DailyMed (National Library of Medicine), updated Dec 31, 2024
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