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dimethyl fumarate

NDC 70710-1205 · HUMAN PRESCRIPTION DRUG · CAPSULE, DELAYED RELEASE

Labeler / ManufacturerZydus Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA210538
Dosage form / routeCAPSULE, DELAYED RELEASE · ORAL
Active ingredientsDIMETHYL FUMARATE (240 mg/1)
Marketing started20200928
Package count2

External sources

Source: openFDA. Public-domain (CC0).