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
- 33342-349_ef3e9cf5-b172-4e67-b621-dc94e9e9d93f
- Product NDC
- 33342-349
- Form
- CAPSULE, DELAYED RELEASE
- Composition / generic term
- Dimethyl Fumarate
- Labeler
- Macleods Pharmaceuticals Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20240626
- Source listing expiry
- 20261231
Source-listed ingredients
- DIMETHYL FUMARATE — 120 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (33342-349-09) · 33342-349-09
- 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE (33342-349-94) · 33342-349-94
- 1 BLISTER PACK in 1 CARTON (33342-349-97) / 14 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK · 33342-349-97
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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