dimethyl fumarate

Generic: dimethyl fumarate

Labeler: zydus lifesciences limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name dimethyl fumarate
Generic Name dimethyl fumarate
Labeler zydus lifesciences limited
Dosage Form CAPSULE, DELAYED RELEASE
Routes
ORAL
Active Ingredients

dimethyl fumarate 120 mg/1

Manufacturer
Zydus Lifesciences Limited

Identifiers & Regulatory

Product NDC 70771-1530
Product ID 70771-1530_d8dceb92-b903-4b29-b3e6-4651fbc598fe
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210538
Listing Expiration 2026-12-31
Marketing Start 2020-09-28

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 707711530
Hyphenated Format 70771-1530

Supplemental Identifiers

RxCUI
1373483 1373491 1373497
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 ANDA210538 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 120 mg/1
source: ndc
Packaging
  • 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70771-1530-7)
source: ndc

Packages (1)

70771-1530-7 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70771-1530-7)

Ingredients (1)

dimethyl fumarate (120 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": "d8dceb92-b903-4b29-b3e6-4651fbc598fe", "openfda": {"unii": ["FO2303MNI2"], "rxcui": ["1373483", "1373491", "1373497"], "spl_set_id": ["7203a262-de0f-42dd-b4fb-8856758b82e9"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": true, "description": "14 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70771-1530-7)", "package_ndc": "70771-1530-7", "marketing_start_date": "20200928"}], "brand_name": "dimethyl fumarate", "product_id": "70771-1530_d8dceb92-b903-4b29-b3e6-4651fbc598fe", "dosage_form": "CAPSULE, DELAYED RELEASE", "product_ndc": "70771-1530", "generic_name": "dimethyl fumarate", "labeler_name": "Zydus Lifesciences Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "dimethyl fumarate", "active_ingredients": [{"name": "DIMETHYL FUMARATE", "strength": "120 mg/1"}], "application_number": "ANDA210538", "marketing_category": "ANDA", "marketing_start_date": "20200928", "listing_expiration_date": "20261231"}