NDC 82249-702
Dalfampridine 10 mg tablet, film coated, extended release
On the label: CivicaScript LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Alkem Laboratories Limited | Baddi Solan, India | Makes it, tests it and packages it | Problems found, fixed voluntarilyMar 27, 2024 · 9 inspections |
Product details
- Generic drug
- Dalfampridine: every company that makes it
- Form
- tablet, film coated, extended release, oral
- Strength
- 10 mg
- Approval
- ANDA ANDA206765
- On the market since
- Jul 21, 2025
- Package NDCs
82249-702-60- Official label
- DailyMed (National Library of Medicine), updated Jul 16, 2025
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