NDC 16729-342 – Fingolimod Hydrochloride

Fingolimod Hydrochloride .5 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC16729-342

Product details

Brand name
Fingolimod Hydrochloride
Generic name
Fingolimod Hydrochloride
Labeler
Accord Healthcare Inc.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA207991
Marketed since
October 18, 2022
Listing expires
December 31, 2026
Pharmacologic class
Sphingosine 1-phosphate Receptor Modulator

Active ingredients

Uses, dosage, side effects and warnings for Fingolimod Hydrochloride →

Package NDC codes (1)

Package NDCDescriptionSince
16729-342-1030 CAPSULE in 1 BOTTLE (16729-342-10)Oct 18, 2022