NDC 69238-1319 – Dimethyl Fumarate

Dimethyl Fumarate 240 mg/1 · Capsule, Delayed Release · Oral

Human Prescription Drug

Product NDC69238-1319

Product details

Brand name
Dimethyl Fumarate
Generic name
Dimethyl Fumarate
Labeler
Amneal Pharmaceuticals NY LLC
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA210402
Marketed since
September 28, 2020
Listing expires
December 31, 2026

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
69238-1319-61 BOTTLE in 1 CARTON (69238-1319-6) / 60 CAPSULE, DELAYED RELEASE in 1 BOTTLESep 28, 2020

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