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Dalfampridine

NDC 16729-292, Dalfampridine, tablet, film coated, extended release, from Accord Healthcare Inc..

Product NDC
16729-292
Status
Listed
Labeler
Accord Healthcare Inc.
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA206863
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/16729-292 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DALFAMPRIDINE10 mg/1

Pharmacologic classes

Potassium Channel Antagonists [MoA]; Potassium Channel Blocker [EPC]

Package NDCNDC-11Package
16729-292-121672902921260 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (16729-292-12)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/354a97e8-35c8-418b-91b2-9e8e066cec65
  • NADAC price for package 16729029212

    GET /v1/drugs/nadac/16729029212

Use it

Look up 16729-292 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/16729-292 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 16729-292. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.