NDC 0480-7820 – Fingolimod

Fingolimod Hydrochloride .5 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC0480-7820

Product details

Brand name
Fingolimod
Generic name
Fingolimod
Labeler
Teva Pharmaceuticals, Inc.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA208008
Marketed since
February 14, 2024
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
0480-7820-5630 CAPSULE in 1 BOTTLE (0480-7820-56)Feb 14, 2024

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