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dimethyl fumarate

NDC 70771-1531, dimethyl fumarate, capsule, delayed release, from Zydus Lifesciences Limited.

Product NDC
70771-1531
Status
Listed
Labeler
Zydus Lifesciences Limited
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/70771-1531 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DIMETHYL FUMARATE240 mg/1
Package NDCNDC-11Package
70771-1531-67077115310660 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70771-1531-6)
70771-1531-87077115310846 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70771-1531-8)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/7203a262-de0f-42dd-b4fb-8856758b82e9

Use it

Look up 70771-1531 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1531 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70771-1531. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.