# Dimethyl Fumarate

NDC: 69539-043
Generic name: Dimethyl fumarate
Labeler / Manufacturer: MSN LABORATORIES PRIVATE LIMITED
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, DELAYED RELEASE
Routes: ORAL
Marketing started: 20200928

FDA application: ANDA210460

## 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:"69539-043"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69539-043
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=074d2820-6cb4-437a-8f6f-a21cb0a8ee02