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Dimethyl Fumarate

NDC 33342-349 · HUMAN PRESCRIPTION DRUG · CAPSULE, DELAYED RELEASE

Labeler / ManufacturerMacleods Pharmaceuticals Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA210377
Dosage form / routeCAPSULE, DELAYED RELEASE · ORAL
Active ingredientsDIMETHYL FUMARATE (120 mg/1)
Marketing started20240626
Package count3

External sources

Source: openFDA. Public-domain (CC0).