NDC 50090-7682

Buspirone Hydrochloride 5 mg tablet

On the label: A-S Medication Solutions. It's repackaged: A-S Medication Solutions rebottles it from Oxford Pharmaceuticals, LLC's NDC 69584-091.

United States: 1

Where the pills inside were made

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

Repackaging site

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
5 mg
Approval
ANDA ANDA075388
On the market since
Jul 27, 2020
Package NDCs
50090-7682-1 50090-7682-2
Official label
DailyMed (National Library of Medicine), updated Oct 9, 2025

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