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Drug company (FDA labeler)

Celgene Corporation

NDC labeler code: 59572

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

23Products (NDC)

Prescription medicines

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
September 1, 2020NDA214120 Azacitidine
ONUREG
Bristol
March 25, 2020NDA209899 Ozanimod hydrochloride
ZEPOSIA
Bristol
November 8, 2019BLA761136 Luspatercept
REBLOZYL
Celgene Corp
August 16, 2019NDA212327 Fedratinib hydrochloride
INREBIC
Bristol-Myers
August 1, 2017NDA209606 Enasidenib mesylate
IDHIFA
Bristol Myers Squibb
February 8, 2013NDA204026 Pomalidomide
POMALYST
Bristol
December 27, 2005NDA021880 Lenalidomide
REVLIMID
Bristol Myers Squibb
May 19, 2004NDA050794 Azacitidine
VIDAZA
Bristol-Myers
July 16, 1998NDA020785 Thalidomide
THALOMID
Bristol-Myers

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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