dimethyl fumarate

Generic: dimethyl fumarate

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name dimethyl fumarate
Generic Name dimethyl fumarate
Labeler a-s medication solutions
Dosage Form CAPSULE, DELAYED RELEASE
Routes
ORAL
Active Ingredients

dimethyl fumarate 240 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-5288
Product ID 50090-5288_43b9bf3a-1ec7-4ca5-9931-61528baadc39
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210500
Listing Expiration 2027-12-31
Marketing Start 2020-09-24

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500905288
Hyphenated Format 50090-5288

Supplemental Identifiers

RxCUI
1373491
UNII
FO2303MNI2

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 ANDA210500 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 240 mg/1
source: ndc
Packaging
  • 1 CAPSULE, DELAYED RELEASE in 1 KIT (50090-5288-0)
source: ndc

Packages (1)

50090-5288-0 1 CAPSULE, DELAYED RELEASE in 1 KIT (50090-5288-0)

Ingredients (1)

dimethyl fumarate (240 mg/1)

Linked Drug Pages (1)

DIMETHYL FUMARATE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "43b9bf3a-1ec7-4ca5-9931-61528baadc39", "openfda": {"unii": ["FO2303MNI2"], "rxcui": ["1373491"], "spl_set_id": ["c2b19329-5c1d-4879-85a9-36ffec3ff5cb"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "1 CAPSULE, DELAYED RELEASE in 1 KIT (50090-5288-0)", "package_ndc": "50090-5288-0", "marketing_start_date": "20201023"}], "brand_name": "DIMETHYL FUMARATE", "product_id": "50090-5288_43b9bf3a-1ec7-4ca5-9931-61528baadc39", "dosage_form": "CAPSULE, DELAYED RELEASE", "product_ndc": "50090-5288", "generic_name": "DIMETHYL FUMARATE", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DIMETHYL FUMARATE", "active_ingredients": [{"name": "DIMETHYL FUMARATE", "strength": "240 mg/1"}], "application_number": "ANDA210500", "marketing_category": "ANDA", "marketing_start_date": "20200924", "listing_expiration_date": "20271231"}