NDC 70512-852 – Dimethyl Fumarate

Dimethyl Fumarate 120 mg/1 · Capsule, Delayed Release · Oral

Human Prescription Drug

Product NDC70512-852

Product details

Brand name
Dimethyl Fumarate
Generic name
Dimethyl Fumarate
Labeler
SOLA Pharmaceuticals, LLC
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA210436
Marketed since
January 31, 2023
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Dimethyl fumarate →

Package NDC codes (1)

Package NDCDescriptionSince
70512-852-141 BOTTLE in 1 CARTON (70512-852-14) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLEMar 12, 2023

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