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Dimethyl Fumarate

NDC 70512-852 · HUMAN PRESCRIPTION DRUG · CAPSULE, DELAYED RELEASE

Labeler / ManufacturerSOLA Pharmaceuticals, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA210436
Dosage form / routeCAPSULE, DELAYED RELEASE · ORAL
Active ingredientsDIMETHYL FUMARATE (120 mg/1)
Marketing started20230131
Package count1

External sources

Source: openFDA. Public-domain (CC0).