NDC 82249-385 – Fingolimod

Fingolimod Hydrochloride .5 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC82249-385

Product details

Brand name
Fingolimod
Generic name
Fingolimod
Labeler
CivicaScript LLC
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA208004
Marketed since
June 1, 2026
Listing expires
December 31, 2027
Pharmacologic class
Sphingosine 1-phosphate Receptor Modulator

Active ingredients

Uses, dosage, side effects and warnings for Fingolimod →

Package NDC codes (1)

Package NDCDescriptionSince
82249-385-3030 CAPSULE in 1 BOTTLE (82249-385-30)Jun 1, 2026

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