# Dimethyl Fumarate

NDC: 69238-1319
Generic name: Dimethyl Fumarate
Labeler / Manufacturer: Amneal Pharmaceuticals NY LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, DELAYED RELEASE
Routes: ORAL
Marketing started: 20200928

FDA application: ANDA210402

## 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:"69238-1319"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69238-1319
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4c7626c6-2b1b-4865-818c-0c79c18c049d