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RUFINAMIDE

NDC 68180-804, rufinamide, tablet, film coated, from Lupin Pharmaceuticals, Inc..

Product NDC
68180-804
Status
Listed
Labeler
Lupin Pharmaceuticals, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA204964
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68180-804 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • RUFINAMIDE400 mg/1
Package NDCNDC-11Package
68180-804-1668180080416120 TABLET, FILM COATED in 1 BOTTLE (68180-804-16)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/2c2c8d41-1ae4-453a-b628-954ee0b3be5c

  • NADAC price for package 68180080416

    GET /v1/drugs/nadac/68180080416

Use it

Look up 68180-804 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68180-804 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68180-804. 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.