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Drug company (FDA labeler)

Cephalon, LLC

NDC labeler code: 63459

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

11Products (NDC)

FDA applications for these products

  • NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
  • BLA: Biologics License Application: how a biologic medicine (made from living cells) is approved.
ApprovedApplicationMedicineSponsor
August 29, 2012BLA125294 Filgrastim
GRANIX
Sicor Biotech
March 20, 2008NDA022249 Bendamustine hydrochloride
TREANDA
Cephalon
June 15, 2007NDA021875 Armodafinil
NUVIGIL
Nuvo Pharms
February 1, 2007NDA021777 Cyclobenzaprine hydrochloride
AMRIX
Teva Pharms Intl
September 25, 2000NDA021248 Arsenic trioxide
TRISENOX
Cephalon
December 24, 1998NDA020717 Modafinil
PROVIGIL
Nuvo Pharms

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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