NDC 62756-064 – Fingolimod

Fingolimod Hydrochloride .5 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC62756-064

Product details

Brand name
Fingolimod
Generic name
Fingolimod
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA208014
Marketed since
October 25, 2022
Listing expires
December 31, 2026
Pharmacologic class
Sphingosine 1-phosphate Receptor Modulator

Active ingredients

Uses, dosage, side effects and warnings for Fingolimod →

Package NDC codes (4)

Package NDCDescriptionSince
62756-064-591 BLISTER PACK in 1 CARTON (62756-064-59) / 7 CAPSULE in 1 BLISTER PACKOct 25, 2022
62756-064-8190 CAPSULE in 1 BOTTLE (62756-064-81)Oct 25, 2022
62756-064-8330 CAPSULE in 1 BOTTLE (62756-064-83)Oct 25, 2022
62756-064-962 BLISTER PACK in 1 CARTON (62756-064-96) / 14 CAPSULE in 1 BLISTER PACKOct 25, 2022

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