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DIMETHYL FUMARATE

NDC 43547-024 · HUMAN PRESCRIPTION DRUG · CAPSULE, DELAYED RELEASE

Generic namedimethyl fumarate
Labeler / ManufacturerSolco Healthcare US, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA210414
Dosage form / routeCAPSULE, DELAYED RELEASE · ORAL
Active ingredientsDIMETHYL FUMARATE (120 mg/1)
Marketing started20221018
Package count1

External sources

Source: openFDA. Public-domain (CC0).