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Dimethyl Fumarate

NDC 59651-084, Dimethyl Fumarate, capsule, delayed release, from Aurobindo Pharma Limited.

Product NDC
59651-084
Status
Listed
Labeler
Aurobindo Pharma Limited
Dosage form
CAPSULE, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA210385
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/59651-084 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DIMETHYL FUMARATE240 mg/1
Package NDCNDC-11Package
59651-084-605965100846060 CAPSULE, DELAYED RELEASE in 1 BOTTLE (59651-084-60)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/08f3a987-6571-42b3-854b-186d782b4494

  • NADAC price for package 59651008460

    GET /v1/drugs/nadac/59651008460

Use it

Look up 59651-084 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/59651-084 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 59651-084. 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.