dimethyl fumarate

Generic: dimethyl fumarate

Labeler: macleods pharmaceuticals limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name dimethyl fumarate
Generic Name dimethyl fumarate
Labeler macleods pharmaceuticals limited
Dosage Form KIT
Manufacturer
Macleods Pharmaceuticals Limited

Identifiers & Regulatory

Product NDC 33342-351
Product ID 33342-351_ef3e9cf5-b172-4e67-b621-dc94e9e9d93f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210377
Listing Expiration 2026-12-31
Marketing Start 2024-06-26

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 33342351
Hyphenated Format 33342-351

Supplemental Identifiers

RxCUI
1373483 1373491 1373497
UPC
0333342349095
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 ANDA210377 (source: ndc)
Routes
oral
source: label

Resolved Composition

Strengths
  • 120 mg
  • 240 mg
  • 23 unit
source: label
Packaging
  • 1 KIT in 1 KIT (33342-351-93) * 14 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (33342-349-91) * 23 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (33342-350-92)
source: ndc

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 (33342-351-93)  *  14 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (33342-349-91)  *  23 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (33342-350-92)", "package_ndc": "33342-351-93", "marketing_start_date": "20240626"}], "brand_name": "Dimethyl Fumarate", "product_id": "33342-351_ef3e9cf5-b172-4e67-b621-dc94e9e9d93f", "dosage_form": "KIT", "product_ndc": "33342-351", "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": "20240626", "listing_expiration_date": "20261231"}