FDA NDC Directory · JSON-LD · Markdown

DIMETHYL FUMARATE

NDC 82009-138 · HUMAN PRESCRIPTION DRUG · CAPSULE, DELAYED RELEASE

Labeler / ManufacturerQuallent Pharmaceuticals Health LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA210500
Dosage form / routeCAPSULE, DELAYED RELEASE · ORAL
Active ingredientsDIMETHYL FUMARATE (240 mg/1)
Marketing started20240615
Package count1

External sources

Source: openFDA. Public-domain (CC0).