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Drug company (FDA labeler)

Vanda Pharmaceuticals Inc.

NDC labeler code: 43068

What is a labeler?

The company whose name is on the package and in the FDA’s National Drug Code (NDC) Directory. It may make the medicine itself or sell medicine made by another company. The first part of every NDC code identifies the labeler.

Official FDA data only

Products, approvals and recalls come from the FDA (NDC Directory, Drugs@FDA, enforcement reports). Recalls are linked to this company by the NDC labeler code on the recalled product.

Questions about your medicine: ask your doctor or pharmacist. In an emergency, call 911.

At a glance

25Products (NDC)

Prescription medicines

FDA applications for these products

  • NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
ApprovedApplicationMedicineSponsor
February 20, 2026NDA220358 Milsaperidone
BYSANTI
Vanda Pharms Inc
December 30, 2025NDA220152 Tradipitant
NEREUS
Vanda Pharms Inc
March 18, 2021NDA213498 Ponesimod
PONVORY
Vanda Pharms Inc
December 1, 2020NDA214517 Tasimelteon
HETLIOZ LQ
Vanda Pharms Inc
January 31, 2014NDA205677 Tasimelteon
HETLIOZ
Vanda Pharms Inc
May 6, 2009NDA022192 Iloperidone
FANAPT
Vanda Pharms Inc

The sponsor is the company that holds the FDA application; it can differ from the labeler.

Recall timeline

No recall of these products (by NDC code) appears in the FDA enforcement reports.

Sources

  1. NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  2. Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  3. Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026

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