NDC 70518-4349
Zonisamide 50 mg capsule
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Aurobindo Pharma Limited's NDC 59651-379.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Apl Healthcare Limited | Mahabubnagar, India | Makes it and tests it | No problems foundJan 18, 2023 · 2 inspections |
Product details
- Generic drug
- Zonisamide: every company that makes it
- Form
- capsule, oral
- Strength
- 50 mg
- Approval
- ANDA ANDA077645
- On the market since
- May 30, 2025
- Package NDCs
70518-4349-070518-4349-1- Official label
- DailyMed (National Library of Medicine), updated Sep 8, 2026
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