# DIMETHYL FUMARATE

NDC: 31722-657
Generic name: DIMETHYL FUMARATE
Labeler / Manufacturer: Camber Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, DELAYED RELEASE
Routes: ORAL
Marketing started: 20200924

FDA application: ANDA210500

## 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:"31722-657"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=31722-657
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b856ac70-71cd-477b-95b1-0a6132c260e8