NDC 82009-138 – Dimethyl Fumarate

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

Human Prescription Drug

Product NDC82009-138

Product details

Brand name
Dimethyl Fumarate
Generic name
Dimethyl Fumarate
Labeler
Quallent Pharmaceuticals Health LLC
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA210500
Marketed since
June 15, 2024
Listing expires
December 31, 2026

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
82009-138-601 BOTTLE in 1 CARTON (82009-138-60) / 60 CAPSULE, DELAYED RELEASE in 1 BOTTLEJun 15, 2024

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