United States · FDA National Drug Code directory

DIMETHYL FUMARATE

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
69238-1626_76c5e6b0-c799-45cf-adb6-2d3845639b62
Product NDC
69238-1626
Form
KIT
Composition / generic term
DIMETHYL FUMARATE
Labeler
Amneal Pharmaceuticals NY LLC
Marketing category
ANDA
Marketing start / end (source format)
20200928
Source listing expiry
20261231

Source-listed ingredients

Separate ingredient quantities are not available in this snapshot. Any composition term above is preserved as source text.

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 KIT in 1 KIT (69238-1626-3) * 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC * 46 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC · 69238-1626-3

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

Browse United States records →