# DIMETHYL FUMARATE

NDC: 68462-570
Generic name: dimethyl fumarate kit
Labeler / Manufacturer: Glenmark Pharmaceuticals Inc., USA
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: KIT
Routes: —
Marketing started: 20201006

FDA application: ANDA210309

## Active ingredients

—

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68462-570"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68462-570
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c3f65da9-f5f4-4161-aded-c23b16fd49ed