NDC 70377-019 – Fingolimod

Fingolimod Hydrochloride .5 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC70377-019

Product details

Brand name
Fingolimod
Generic name
Fingolimod
Labeler
Biocon Pharma Inc.
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 (2)

Package NDCDescriptionSince
70377-019-1130 CAPSULE in 1 BOTTLE (70377-019-11)Mar 28, 2024
70377-019-2128 CAPSULE in 1 CARTON (70377-019-21)Mar 28, 2024

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