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Dimethyl Fumarate

NDC 33342-351, Dimethyl Fumarate, kit, from Macleods Pharmaceuticals Limited.

Product NDC
33342-351
Status
Listed
Labeler
Macleods Pharmaceuticals Limited
Dosage form
KIT
Route
—
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA210377
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/33342-351 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

None listed.

Package NDCNDC-11Package
33342-351-93333420351931 KIT in 1 KIT (33342-351-93) * 14 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (33342-349-91) * 23 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (33342-350-92)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f8ada3e3-55c0-43e3-95b9-c6d11ffc42dd

Use it

Look up 33342-351 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/33342-351 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 33342-351. 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.