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DIMETHYL FUMARATE

NDC 31722-657, DIMETHYL FUMARATE, capsule, delayed release, from Camber Pharmaceuticals, Inc..

Product NDC
31722-657
Status
Listed
Labeler
Camber Pharmaceuticals, Inc.
Dosage form
CAPSULE, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA210500
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/31722-657 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DIMETHYL FUMARATE120 mg/1
Package NDCNDC-11Package
31722-657-31317220657311 BOTTLE in 1 CARTON (31722-657-31) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE
31722-657-323172206573210 BLISTER PACK in 1 CARTON (31722-657-32) / 10 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b856ac70-71cd-477b-95b1-0a6132c260e8
  • NADAC price for package 31722065731

    GET /v1/drugs/nadac/31722065731

Use it

Look up 31722-657 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/31722-657 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 31722-657. 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.