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DIMETHYL FUMARATE

NDC 31722-658 · HUMAN PRESCRIPTION DRUG · CAPSULE, DELAYED RELEASE

Labeler / ManufacturerCamber Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA210500
Dosage form / routeCAPSULE, DELAYED RELEASE · ORAL
Active ingredientsDIMETHYL FUMARATE (240 mg/1)
Marketing started20200924
Package count3

External sources

Source: openFDA. Public-domain (CC0).