NDC 0121-1016

Atovaquone 750 mg per 5 mL suspension

On the label: Pharmaceutical Associates, Inc..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
PAI Holdings, LLC dba Pharmaceutical Associates, Inc. and dba PAI PharmaGreenville, SC, United StatesMakes it, tests it, packages it and labels it No problems foundAug 1, 2025 · 18 inspections, 1 with FDA action

Product details

Generic drug
Atovaquone: every company that makes it
Form
suspension, oral
Strength
750 mg per 5 mL
Approval
ANDA ANDA214272
On the market since
Jan 10, 2024
Package NDCs
0121-1016-05 0121-1016-18 0121-1016-42
Official label
DailyMed (National Library of Medicine), updated Apr 30, 2026

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