NDC 68382-623

Buspirone hydrochloride 7.5 mg tablet

On the label: Zydus Pharmaceuticals (USA) Inc..

India: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Zydus Lifesciences LimitedAhmedabad, IndiaMakes it and tests it Problems found, fixed voluntarilyAug 5, 2022 · 10 inspections, 3 with FDA action

Product details

Generic drug
Buspirone: every company that makes it
Form
tablet, oral
Strength
7.5 mg
Approval
ANDA ANDA078888
On the market since
Mar 21, 2023
Package NDCs
68382-623-01 68382-623-05 68382-623-10 68382-623-30
Official label
DailyMed (National Library of Medicine), updated Feb 12, 2025

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