NDC 65862-863
Dalfampridine 10 mg tablet, film coated, extended release
On the label: Aurobindo Pharma Limited.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurobindo Pharma Limited | Mahabubnagar, India | Makes it and tests it | Problems found, fixed voluntarilyMay 10, 2022 · 7 inspections, 1 with FDA action |
Product details
- Generic drug
- Dalfampridine: every company that makes it
- Form
- tablet, film coated, extended release, oral
- Strength
- 10 mg
- Approval
- ANDA ANDA206811
- On the market since
- Jun 25, 2018
- Package NDCs
65862-863-0165862-863-0565862-863-60- Official label
- DailyMed (National Library of Medicine), updated Feb 15, 2024
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