dimethyl fumarate
Generic: dimethyl fumarate
Labeler: amneal pharmaceuticals ny llcDrug Facts
Product Profile
Brand Name
dimethyl fumarate
Generic Name
dimethyl fumarate
Labeler
amneal pharmaceuticals ny llc
Dosage Form
KIT
Manufacturer
Identifiers & Regulatory
Product NDC
69238-1626
Product ID
69238-1626_76c5e6b0-c799-45cf-adb6-2d3845639b62
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA210402
Listing Expiration
2026-12-31
Marketing Start
2020-09-28
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
692381626
Hyphenated Format
69238-1626
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
ANDA210402 (source: ndc)
Routes
source: label
Resolved Composition
Strengths
- 120 mg
- 240 mg
Packaging
- 1 KIT in 1 KIT (69238-1626-3) * 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC * 46 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC
Packages (1)
Ingredients (0)
No ingredient records.
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"spl_id": "76c5e6b0-c799-45cf-adb6-2d3845639b62", "openfda": {"upc": ["0369238131963", "0369238162639", "0369238162684"], "unii": ["FO2303MNI2"], "rxcui": ["1373483", "1373491", "1373497"], "spl_set_id": ["4c7626c6-2b1b-4865-818c-0c79c18c049d"], "manufacturer_name": ["Amneal Pharmaceuticals NY LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 KIT (69238-1626-3) * 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC * 46 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC", "package_ndc": "69238-1626-3", "marketing_start_date": "20200928"}], "brand_name": "DIMETHYL FUMARATE", "product_id": "69238-1626_76c5e6b0-c799-45cf-adb6-2d3845639b62", "dosage_form": "KIT", "product_ndc": "69238-1626", "generic_name": "DIMETHYL FUMARATE", "labeler_name": "Amneal Pharmaceuticals NY LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DIMETHYL FUMARATE", "application_number": "ANDA210402", "marketing_category": "ANDA", "marketing_start_date": "20200928", "listing_expiration_date": "20261231"}