dimethyl fumarate
Generic: dimethyl fumarate
Labeler: cipla usa inc.Drug Facts
Product Profile
Brand Name
dimethyl fumarate
Generic Name
dimethyl fumarate
Labeler
cipla usa inc.
Dosage Form
CAPSULE, DELAYED RELEASE
Routes
Active Ingredients
dimethyl fumarate 120 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
69097-322
Product ID
69097-322_d64e8be8-de52-40c2-8730-bef67c6b0914
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA210305
Listing Expiration
2026-12-31
Marketing Start
2020-09-24
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
69097322
Hyphenated Format
69097-322
Supplemental Identifiers
RxCUI
UPC
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 (source: ndc)
Application Number
ANDA210305 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 120 mg/1
Packaging
- 1 BOTTLE, PLASTIC in 1 CARTON (69097-322-89) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "d64e8be8-de52-40c2-8730-bef67c6b0914", "openfda": {"upc": ["0369097323035", "0369097322892", "0369097323882", "0369097552039"], "unii": ["FO2303MNI2"], "rxcui": ["1373483", "1373491", "1373497"], "spl_set_id": ["6c42107a-2a42-4263-97b6-ae0d7675c92a"], "manufacturer_name": ["Cipla USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (69097-322-89) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC", "package_ndc": "69097-322-89", "marketing_start_date": "20200924"}], "brand_name": "DIMETHYL FUMARATE", "product_id": "69097-322_d64e8be8-de52-40c2-8730-bef67c6b0914", "dosage_form": "CAPSULE, DELAYED RELEASE", "product_ndc": "69097-322", "generic_name": "DIMETHYL FUMARATE", "labeler_name": "Cipla USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DIMETHYL FUMARATE", "active_ingredients": [{"name": "DIMETHYL FUMARATE", "strength": "120 mg/1"}], "application_number": "ANDA210305", "marketing_category": "ANDA", "marketing_start_date": "20200924", "listing_expiration_date": "20261231"}