Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Kvk-Tech, Inc. | Newtown, PA, United States | Makes it | Serious problems, FDA actionMar 14, 2025 · 13 inspections, 3 with FDA action |
Recalls
- Jul 2, 2021 · Class I · KVK-Tech, Inc.
Temperature abuse: the firm received customer complaints of unusual grittiness in the product.
Lots: Batch # 16653A, 16654A, Exp 12/2022
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 ANDA210510
- On the market since
- Mar 29, 2019
- Package NDCs
10702-223-21- Official label
- DailyMed (National Library of Medicine), updated Jun 16, 2026
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