# Dimethyl fumarate

NDC: 82249-747
Generic name: Dimethyl fumarate
Labeler / Manufacturer: CivicaScript LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, DELAYED RELEASE
Routes: ORAL
Marketing started: 20250611

FDA application: ANDA210440

## Active ingredients

- DIMETHYL FUMARATE: 240 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"82249-747"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=82249-747
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f3002b6a-841e-4247-9155-3acfb30cabcd