NDC 82804-964
Buspirone Hydrochloride 30 mg tablet
On the label: Proficient Rx LP. It's repackaged: Proficient Rx LP rebottles it from Oxford Pharmaceuticals, LLC's NDC 69584-094.
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
- Proficient Rx LP, Thousand Oaks, 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
- 30 mg
- Approval
- ANDA ANDA078302
- On the market since
- May 1, 2020
- Package NDCs
82804-964-0082804-964-1182804-964-3082804-964-5582804-964-6082804-964-7282804-964-90- Official label
- DailyMed (National Library of Medicine), updated Jan 1, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?