NDC 65862-952 – Fingolimod

Fingolimod Hydrochloride .5 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC65862-952

Product details

Brand name
Fingolimod
Generic name
Fingolimod
Labeler
Aurobindo Pharma Limited
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA207983
Marketed since
February 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 (3)

Package NDCDescriptionSince
65862-952-071 BLISTER PACK in 1 CARTON (65862-952-07) / 7 CAPSULE in 1 BLISTER PACKFeb 28, 2024
65862-952-284 BLISTER PACK in 1 CARTON (65862-952-28) / 7 CAPSULE in 1 BLISTER PACKFeb 28, 2024
65862-952-3030 CAPSULE in 1 BOTTLE (65862-952-30)Feb 28, 2024

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