NDC 71335-1752
Buspirone Hydrochloride 15 mg tablet
On the label: Bryant Ranch Prepack. It's repackaged: Bryant Ranch Prepack rebottles it from Oxford Pharmaceuticals, LLC's NDC 69584-093.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Oxford Pharmaceuticals, LLC | Birmingham, AL, United States | Makes it | Problems found, fixed voluntarilyNov 3, 2023 · 3 inspections |
Repackaging site
- Bryant Ranch Prepack, Burbank, CA, United States · repackages it and relabels it
Recalls
- May 5, 2021 · Class II · Oxford Pharmaceuticals, LLC
Presence of Foreign Tablets/Capsules
Lots: Lot #: C21021A, Exp. 03/2023
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Buspirone: every company that makes it
- Form
- tablet, oral
- Strength
- 15 mg
- Approval
- ANDA ANDA075388
- On the market since
- Jul 27, 2020
- Package NDCs
71335-1752-171335-1752-271335-1752-371335-1752-471335-1752-571335-1752-671335-1752-7- Official label
- DailyMed (National Library of Medicine), updated Oct 1, 2025
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