dimethyl fumarate
Generic: dimethyl fumarate kit
Labeler: glenmark pharmaceuticals inc., usaDrug Facts
Product Profile
Brand Name
dimethyl fumarate
Generic Name
dimethyl fumarate kit
Labeler
glenmark pharmaceuticals inc., usa
Dosage Form
KIT
Manufacturer
Identifiers & Regulatory
Product NDC
68462-570
Product ID
68462-570_74611591-657b-40e8-8ae1-1e5533a05d97
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA210309
Listing Expiration
2026-12-31
Marketing Start
2020-10-06
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
68462570
Hyphenated Format
68462-570
Supplemental Identifiers
RxCUI
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 kit (source: ndc)
Application Number
ANDA210309 (source: ndc)
Routes
source: label
Resolved Composition
Strengths
- 120 mg
- 240 mg
Packaging
- 1 KIT in 1 KIT (68462-570-78) * 14 CAPSULE in 1 BOTTLE * 46 CAPSULE in 1 BOTTLE
Packages (1)
Ingredients (0)
No ingredient records.
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"spl_id": "74611591-657b-40e8-8ae1-1e5533a05d97", "openfda": {"unii": ["FO2303MNI2"], "rxcui": ["1373483", "1373491", "1373497"], "spl_set_id": ["c3f65da9-f5f4-4161-aded-c23b16fd49ed"], "manufacturer_name": ["Glenmark Pharmaceuticals Inc., USA"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 KIT (68462-570-78) * 14 CAPSULE in 1 BOTTLE * 46 CAPSULE in 1 BOTTLE", "package_ndc": "68462-570-78", "marketing_start_date": "20201006"}], "brand_name": "DIMETHYL FUMARATE", "product_id": "68462-570_74611591-657b-40e8-8ae1-1e5533a05d97", "dosage_form": "KIT", "product_ndc": "68462-570", "generic_name": "dimethyl fumarate kit", "labeler_name": "Glenmark Pharmaceuticals Inc., USA", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DIMETHYL FUMARATE", "application_number": "ANDA210309", "marketing_category": "ANDA", "marketing_start_date": "20201006", "listing_expiration_date": "20261231"}