NDC 70771-1603 – Fingolimod

Fingolimod Hydrochloride .5 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC70771-1603

Product details

Brand name
Fingolimod
Generic name
Fingolimod
Labeler
Zydus Lifesciences Limited
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
70771-1603-1100 CAPSULE in 1 BOTTLE (70771-1603-1)Oct 11, 2022
70771-1603-330 CAPSULE in 1 BOTTLE (70771-1603-3)Oct 11, 2022
70771-1603-71 BLISTER PACK in 1 CARTON (70771-1603-7) / 7 CAPSULE in 1 BLISTER PACKOct 11, 2022
70771-1603-84 BLISTER PACK in 1 CARTON (70771-1603-8) / 7 CAPSULE in 1 BLISTER PACKOct 11, 2022
70771-1603-990 CAPSULE in 1 BOTTLE (70771-1603-9)Oct 11, 2022

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