NDC 69452-252

Atovaquone 750 mg per 5 mL suspension

On the label: Bionpharma Inc..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Corerx, Inc.Clearwater, FL, United StatesMakes it Problems found, fixed voluntarilyFeb 26, 2026 · 5 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
Atovaquone: every company that makes it
Form
suspension, oral
Strength
750 mg per 5 mL
Approval
ANDA ANDA212918
On the market since
Jun 1, 2021
Package NDCs
69452-252-87
Official label
DailyMed (National Library of Medicine), updated Dec 4, 2025

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