United States · FDA National Drug Code directory
AMPYRA
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 10144-427_dda9045d-2f23-412c-9543-74832f421739
- Product NDC
- 10144-427
- Form
- TABLET, FILM COATED, EXTENDED RELEASE
- Composition / generic term
- Dalfampridine
- Labeler
- Merz Pharmaceuticals, LLC
- Marketing category
- NDA
- Marketing start / end (source format)
- 20100301
- Source listing expiry
- 20271231
Source-listed ingredients
- DALFAMPRIDINE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (10144-427-60) · 10144-427-60
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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