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dimethyl fumarate

NDC 70710-1204, dimethyl fumarate, capsule, delayed release, from Zydus Pharmaceuticals USA Inc..

Product NDC
70710-1204
Status
Listed
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
CAPSULE, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA210538
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70710-1204 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DIMETHYL FUMARATE120 mg/1
Package NDCNDC-11Package
70710-1204-77071012040714 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70710-1204-7)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/e7ef9b9e-d97a-4a56-b792-a1a255613156

Use it

Look up 70710-1204 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70710-1204 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70710-1204. 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.