FDA NDC Directory · JSON-LD · Markdown

DIMETHYL FUMARATE

NDC 68462-570 · HUMAN PRESCRIPTION DRUG · KIT

Generic namedimethyl fumarate kit
Labeler / ManufacturerGlenmark Pharmaceuticals Inc., USA
Marketing categoryAbbreviated NDA (generic) · App ANDA210309
Dosage form / routeKIT
Active ingredients—
Marketing started20201006
Package count1

External sources

Source: openFDA. Public-domain (CC0).