dimethyl fumarate

Generic: dimethyl fumarate

Labeler: camber pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name dimethyl fumarate
Generic Name dimethyl fumarate
Labeler camber pharmaceuticals, inc.
Dosage Form CAPSULE, DELAYED RELEASE
Routes
ORAL
Active Ingredients

dimethyl fumarate 240 mg/1

Manufacturer
Camber Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 31722-658
Product ID 31722-658_1814ba82-76cc-c580-e063-6294a90a5e57
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210500
Listing Expiration 2026-12-31
Marketing Start 2020-09-24

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 31722658
Hyphenated Format 31722-658

Supplemental Identifiers

RxCUI
1373483 1373491 1373497
UPC
0331722657310 0331722658324 0331722658317
UNII
FO2303MNI2

Packaging Origin

Original Packager
true

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 BOTTLE in 1 CARTON (31722-658-31) / 46 CAPSULE, DELAYED RELEASE in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (31722-658-32) / 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE
  • 10 BLISTER PACK in 1 CARTON (31722-658-33) / 10 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK
source: ndc

Packages (3)

31722-658-31 1 BOTTLE in 1 CARTON (31722-658-31) / 46 CAPSULE, DELAYED RELEASE in 1 BOTTLE 31722-658-32 1 BOTTLE in 1 CARTON (31722-658-32) / 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE 31722-658-33 10 BLISTER PACK in 1 CARTON (31722-658-33) / 10 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK

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": "1814ba82-76cc-c580-e063-6294a90a5e57", "openfda": {"upc": ["0331722657310", "0331722658324", "0331722658317"], "unii": ["FO2303MNI2"], "rxcui": ["1373483", "1373491", "1373497"], "spl_set_id": ["b856ac70-71cd-477b-95b1-0a6132c260e8"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (31722-658-31)  / 46 CAPSULE, DELAYED RELEASE in 1 BOTTLE", "package_ndc": "31722-658-31", "marketing_start_date": "20200924"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (31722-658-32)  / 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE", "package_ndc": "31722-658-32", "marketing_start_date": "20200924"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (31722-658-33)  / 10 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK", "package_ndc": "31722-658-33", "marketing_start_date": "20200924"}], "brand_name": "DIMETHYL FUMARATE", "product_id": "31722-658_1814ba82-76cc-c580-e063-6294a90a5e57", "dosage_form": "CAPSULE, DELAYED RELEASE", "product_ndc": "31722-658", "generic_name": "DIMETHYL FUMARATE", "labeler_name": "Camber Pharmaceuticals, Inc.", "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": "20261231"}