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Rufinamide

NDC 0054-0426, Rufinamide, tablet, film coated, from Hikma Pharmaceuticals USA Inc..

Product NDC
0054-0426
Status
Listed
Labeler
Hikma Pharmaceuticals USA Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA204988
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0054-0426 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • RUFINAMIDE400 mg/1
Package NDCNDC-11Package
0054-0426-2300054042623120 TABLET, FILM COATED in 1 BOTTLE (0054-0426-23)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/56316809-6e73-4717-990b-fc84bf6bf433

  • NADAC price for package 00054042623

    GET /v1/drugs/nadac/00054042623

Use it

Look up 0054-0426 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0054-0426 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0054-0426. 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.