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
69539-240_1e7672d0-2532-401b-81a2-dd76968d2745
Product NDC
69539-240
Form
KIT
Composition / generic term
Dimethyl Fumarate
Labeler
MSN LABORATORIES PRIVATE LIMITED
Marketing category
ANDA
Marketing start / end (source format)
20210520
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 (69539-240-18) * 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE * 46 CAPSULE, DELAYED RELEASE in 1 BOTTLE · 69539-240-18

Source and coverage

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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.

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