# DIMETHYL FUMARATE

NDC: 43547-024
Generic name: dimethyl fumarate
Labeler / Manufacturer: Solco Healthcare US, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, DELAYED RELEASE
Routes: ORAL
Marketing started: 20221018

FDA application: ANDA210414

## Active ingredients

- DIMETHYL FUMARATE: 120 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"43547-024"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43547-024
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a3677dce-a44b-481f-8a76-9ff3a4d42105