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Drug company (FDA labeler)

NextWave Pharmaceuticals, Inc

NDC labeler code: 24478

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

13Products (NDC)

Prescription medicines

FDA applications for these products

  • NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
ApprovedApplicationMedicineSponsor
May 24, 2024NDA217645 Clonidine
ONYDA XR
Tris Pharma Inc
November 4, 2021NDA210526 Amphetamine
DYANAVEL XR 10, DYANAVEL XR 15, DYANAVEL XR 20
Tris Pharma Inc
December 4, 2015NDA207960 Methylphenidate
QUILLICHEW ER
Nextwave Pharms
October 19, 2015NDA208147 Amphetamine
DYANAVEL XR
Tris Pharma Inc
September 27, 2012NDA202100 Methylphenidate
QUILLIVANT XR
Nextwave

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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