NDC 68462-421
atovaquone 750 mg per 5 mL suspension
On the label: Glenmark Pharmaceuticals Inc., USA.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Glenmark Pharmaceuticals Limited | Solan, India | Makes it and tests it | Serious problems, FDA actionJun 22, 2022 · 6 inspections, 1 with FDA action |
| PPL Healthcare LLC | Sellersville, PA, United States | Makes it | Problems found, fixed voluntarilyMay 8, 2026 · 9 inspections |
Product details
- Generic drug
- Atovaquone: every company that makes it
- Form
- suspension, oral
- Strength
- 750 mg per 5 mL
- Approval
- ANDA ANDA209685
- On the market since
- Dec 31, 2017
- Package NDCs
68462-421-2168462-421-69- Official label
- DailyMed (National Library of Medicine), updated May 6, 2026
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