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DIMETHYL FUMARATE

NDC 31722-680 · HUMAN PRESCRIPTION DRUG · KIT

Generic namedimethyl fumarate
Labeler / ManufacturerCamber Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA210500
Dosage form / routeKIT
Active ingredients—
Marketing started20200924
Package count1

External sources

Source: openFDA. Public-domain (CC0).