NDC 31722-658 – Dimethyl Fumarate

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

Human Prescription Drug

Product NDC31722-658

Product details

Brand name
Dimethyl Fumarate
Generic name
Dimethyl Fumarate
Labeler
Camber Pharmaceuticals, Inc.
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA210500
Marketed since
September 24, 2020
Listing expires
December 31, 2026

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
31722-658-311 BOTTLE in 1 CARTON (31722-658-31) / 46 CAPSULE, DELAYED RELEASE in 1 BOTTLESep 24, 2020
31722-658-321 BOTTLE in 1 CARTON (31722-658-32) / 60 CAPSULE, DELAYED RELEASE in 1 BOTTLESep 24, 2020
31722-658-3310 BLISTER PACK in 1 CARTON (31722-658-33) / 10 CAPSULE, DELAYED RELEASE in 1 BLISTER PACKSep 24, 2020

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