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Dalfampridine

NDC 82249-702, Dalfampridine, tablet, film coated, extended release, from CivicaScript LLC.

Product NDC
82249-702
Status
Listed
Labeler
CivicaScript LLC
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA206765
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/82249-702 \
  -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
82249-702-608224907026060 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (82249-702-60)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c40dcc84-b839-44aa-94f2-886fb1c3d75c

  • NADAC price for package 82249070260

    GET /v1/drugs/nadac/82249070260

Use it

Look up 82249-702 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/82249-702 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 82249-702. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.