NDC 82804-039
Buspirone Hydrochloride 7.5 mg tablet
On the label: Proficient Rx LP. It's repackaged: Proficient Rx LP rebottles it from Aurobindo Pharma Limited's NDC 59651-390.
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
- Proficient Rx LP, Thousand Oaks, CA, United States · repackages it and relabels it
Product details
- Generic drug
- Buspirone: every company that makes it
- Form
- tablet, oral
- Strength
- 7.5 mg
- Approval
- ANDA ANDA078246
- On the market since
- Feb 21, 2020
- Package NDCs
82804-039-2082804-039-3082804-039-6082804-039-90- Official label
- DailyMed (National Library of Medicine), updated Feb 1, 2024
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