NDC 71335-2073
Buspirone Hydrochloride 15 mg tablet
On the label: Bryant Ranch Prepack. It's repackaged: Bryant Ranch Prepack rebottles it from Aurobindo Pharma Limited's NDC 59651-392.
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
- 15 mg
- Approval
- ANDA ANDA078246
- On the market since
- Feb 21, 2020
- Package NDCs
71335-2073-171335-2073-271335-2073-371335-2073-471335-2073-571335-2073-671335-2073-7- Official label
- DailyMed (National Library of Medicine), updated Jun 5, 2023
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