NDC 82009-143 – Fingolimod

Fingolimod Hydrochloride .5 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC82009-143

Product details

Brand name
Fingolimod
Generic name
Fingolimod
Labeler
Quallent Pharmaceuticals Health LLC
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA207979
Marketed since
March 28, 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
82009-143-3030 CAPSULE in 1 BOTTLE (82009-143-30)Mar 28, 2024

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