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.
Prescription medicines
- LenalidomideRevlimid · 6 products
- ThalidomideThalomid · 4 products
- PomalidomidePomalyst · 4 products
- AzacitidineOnureg, Vidaza · 3 products
- Enasidenib mesylateIdhifa · 2 products
- LuspaterceptReblozyl · 2 products
- Fedratinib hydrochlorideInrebic · 1 product
- Ozanimod hydrochlorideZeposia · 1 product
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.
| Approved | Application | Medicine | Sponsor |
|---|---|---|---|
| September 1, 2020 | NDA214120 | Azacitidine ONUREG | Bristol |
| March 25, 2020 | NDA209899 | Ozanimod hydrochloride ZEPOSIA | Bristol |
| November 8, 2019 | BLA761136 | Luspatercept REBLOZYL | Celgene Corp |
| August 16, 2019 | NDA212327 | Fedratinib hydrochloride INREBIC | Bristol-Myers |
| August 1, 2017 | NDA209606 | Enasidenib mesylate IDHIFA | Bristol Myers Squibb |
| February 8, 2013 | NDA204026 | Pomalidomide POMALYST | Bristol |
| December 27, 2005 | NDA021880 | Lenalidomide REVLIMID | Bristol Myers Squibb |
| May 19, 2004 | NDA050794 | Azacitidine VIDAZA | Bristol-Myers |
| July 16, 1998 | NDA020785 | 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.
Next steps
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Sources
- NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026