NDC 71610-206

Buspirone hydrochloride 15 mg tablet

On the label: Aphena Pharma Solutions - Tennessee, Inc.. It's repackaged: Aphena Pharma Solutions - Tennessee, Inc. rebottles it from Zydus Pharmaceuticals (USA) Inc.'s NDC 68382-182.

India: 1

Where the pills inside were made

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

Repackaging site

Product details

Generic drug
Buspirone: every company that makes it
Form
tablet, oral
Strength
15 mg
Approval
ANDA ANDA078888
On the market since
May 3, 2014
Package NDCs
71610-206-30
Official label
DailyMed (National Library of Medicine), updated Dec 19, 2018

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