NDC 71335-2081
Buspirone Hydrochloride 10 mg tablet
On the label: Bryant Ranch Prepack. It's repackaged: Bryant Ranch Prepack rebottles it from Aurobindo Pharma Limited's NDC 59651-391.
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
- Bryant Ranch Prepack, Burbank, CA, United States · repackages it and relabels it
Product details
- Generic drug
- Buspirone: every company that makes it
- Form
- tablet, oral
- Strength
- 10 mg
- Approval
- ANDA ANDA078246
- On the market since
- Feb 21, 2020
- Package NDCs
71335-2081-171335-2081-271335-2081-371335-2081-471335-2081-571335-2081-6- Official label
- DailyMed (National Library of Medicine), updated Nov 28, 2023
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