NDC 69584-094

Buspirone Hydrochloride 30 mg tablet

On the label: Oxford Pharmaceuticals, LLC.

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Oxford Pharmaceuticals, LLCBirmingham, AL, United StatesMakes it Problems found, fixed voluntarilyNov 3, 2023 · 3 inspections

Recalls

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
69584-094-06 69584-094-18 69584-094-50
Official label
DailyMed (National Library of Medicine), updated Aug 14, 2025

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