# Dimethyl Fumarate

NDC: 70512-853
Generic name: Dimethyl Fumarate
Labeler / Manufacturer: SOLA Pharmaceuticals, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, DELAYED RELEASE
Routes: ORAL
Marketing started: 20230131

FDA application: ANDA210436

## 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:"70512-853"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70512-853
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b4a200c1-f25a-4aa8-8770-06182fdeda9d