FDA NDC Directory · JSON-LD · Markdown

Dimethyl Fumarate

NDC 69539-042 · HUMAN PRESCRIPTION DRUG · CAPSULE, DELAYED RELEASE

Generic nameDimethyl fumarate
Labeler / ManufacturerMSN LABORATORIES PRIVATE LIMITED
Marketing categoryAbbreviated NDA (generic) · App ANDA210460
Dosage form / routeCAPSULE, DELAYED RELEASE · ORAL
Active ingredientsDIMETHYL FUMARATE (120 mg/1)
Marketing started20200928
Package count2

External sources

Source: openFDA. Public-domain (CC0).