NDC 77771-235

Buspirone hydrochloride 7.5 mg tablet

On the label: Radha Pharmaceuticals, Inc..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
A&Z Pharmaceutical, Inc.Hauppauge, NY, United StatesMakes it Problems found, fixed voluntarilySep 26, 2025 · 4 inspections

Product details

Generic drug
Buspirone: every company that makes it
Form
tablet, oral
Strength
7.5 mg
Approval
ANDA ANDA202087
On the market since
Sep 18, 2025
Package NDCs
77771-235-01
Official label
DailyMed (National Library of Medicine), updated Sep 22, 2025

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