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DIMETHYL FUMARATE

NDC 69097-322, DIMETHYL FUMARATE, capsule, delayed release, from Cipla USA Inc..

Product NDC
69097-322
Status
Listed
Labeler
Cipla USA Inc.
Dosage form
CAPSULE, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA210305
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69097-322 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DIMETHYL FUMARATE120 mg/1
Package NDCNDC-11Package
69097-322-89690970322891 BOTTLE, PLASTIC in 1 CARTON (69097-322-89) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/6c42107a-2a42-4263-97b6-ae0d7675c92a

  • NADAC price for package 69097032289

    GET /v1/drugs/nadac/69097032289

Use it

Look up 69097-322 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69097-322 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69097-322. 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.