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Dimethyl fumarate

NDC 67877-556 · HUMAN PRESCRIPTION DRUG · CAPSULE, DELAYED RELEASE

Labeler / ManufacturerAscend Laboratories, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA210440
Dosage form / routeCAPSULE, DELAYED RELEASE · ORAL
Active ingredientsDIMETHYL FUMARATE (240 mg/1)
Marketing started20200926
Package count5

External sources

Source: openFDA. Public-domain (CC0).