# dimethyl fumarate

NDC: 70710-1204
Generic name: dimethyl fumarate
Labeler / Manufacturer: Zydus Pharmaceuticals USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, DELAYED RELEASE
Routes: ORAL
Marketing started: 20200928

FDA application: ANDA210538

## 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:"70710-1204"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70710-1204
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e7ef9b9e-d97a-4a56-b792-a1a255613156