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Dimethyl Fumarate

NDC 70512-852, Dimethyl Fumarate, capsule, delayed release, from SOLA Pharmaceuticals, LLC.

Product NDC
70512-852
Status
Listed
Labeler
SOLA Pharmaceuticals, LLC
Dosage form
CAPSULE, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA210436
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70512-852 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DIMETHYL FUMARATE120 mg/1
Package NDCNDC-11Package
70512-852-14705120852141 BOTTLE in 1 CARTON (70512-852-14) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b4a200c1-f25a-4aa8-8770-06182fdeda9d

  • NADAC price for package 70512085214

    GET /v1/drugs/nadac/70512085214

Use it

Look up 70512-852 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70512-852 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70512-852. 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.