NDC 68382-912 – Fingolimod

Fingolimod Hydrochloride .5 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC68382-912

Product details

Brand name
Fingolimod
Generic name
Fingolimod
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA207994
Marketed since
October 11, 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 (5)

Package NDCDescriptionSince
68382-912-01100 CAPSULE in 1 BOTTLE (68382-912-01)Oct 11, 2022
68382-912-0630 CAPSULE in 1 BOTTLE (68382-912-06)Oct 11, 2022
68382-912-1690 CAPSULE in 1 BOTTLE (68382-912-16)Oct 11, 2022
68382-912-691 BLISTER PACK in 1 CARTON (68382-912-69) / 7 CAPSULE in 1 BLISTER PACKOct 11, 2022
68382-912-704 BLISTER PACK in 1 CARTON (68382-912-70) / 7 CAPSULE in 1 BLISTER PACKOct 11, 2022

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