dimethyl fumarate
Generic: dimethyl fumarate
Labeler: macleods pharmaceuticals limitedDrug Facts
Product Profile
Brand Name
dimethyl fumarate
Generic Name
dimethyl fumarate
Labeler
macleods pharmaceuticals limited
Dosage Form
KIT
Manufacturer
Identifiers & Regulatory
Product NDC
33342-579
Product ID
33342-579_ef3e9cf5-b172-4e67-b621-dc94e9e9d93f
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA210377
Listing Expiration
2026-12-31
Marketing Start
2025-06-27
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
33342579
Hyphenated Format
33342-579
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
dimethyl fumarate (source: ndc)
Generic Name
dimethyl fumarate (source: ndc)
Application Number
ANDA210377 (source: ndc)
Routes
source: label
Resolved Composition
Strengths
- 120 mg
- 240 mg
- 23 unit
Packaging
- 1 KIT in 1 KIT (33342-579-96) * 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE (33342-349-94) * 46 CAPSULE, DELAYED RELEASE in 1 BOTTLE (33342-350-95)
Packages (1)
Ingredients (0)
No ingredient records.
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"spl_id": "ef3e9cf5-b172-4e67-b621-dc94e9e9d93f", "openfda": {"upc": ["0333342349095"], "unii": ["FO2303MNI2"], "rxcui": ["1373483", "1373491", "1373497"], "spl_set_id": ["f8ada3e3-55c0-43e3-95b9-c6d11ffc42dd"], "manufacturer_name": ["Macleods Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 KIT (33342-579-96) * 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE (33342-349-94) * 46 CAPSULE, DELAYED RELEASE in 1 BOTTLE (33342-350-95)", "package_ndc": "33342-579-96", "marketing_start_date": "20250627"}], "brand_name": "Dimethyl Fumarate", "product_id": "33342-579_ef3e9cf5-b172-4e67-b621-dc94e9e9d93f", "dosage_form": "KIT", "product_ndc": "33342-579", "generic_name": "Dimethyl Fumarate", "labeler_name": "Macleods Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dimethyl Fumarate", "application_number": "ANDA210377", "marketing_category": "ANDA", "marketing_start_date": "20250627", "listing_expiration_date": "20261231"}