United States · FDA National Drug Code directory

PONVORY

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
43068-620_5280b437-62d4-417f-bd65-eb8944a85166
Product NDC
43068-620
Form
TABLET, FILM COATED
Composition / generic term
Ponesimod
Labeler
Vanda Pharmaceuticals Inc.
Marketing category
NDA
Marketing start / end (source format)
20210318
Source listing expiry
20261231

Source-listed ingredients

  • PONESIMOD — 20 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 BOTTLE in 1 CARTON (43068-620-01) / 30 TABLET, FILM COATED in 1 BOTTLE · 43068-620-01

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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