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Drug company (FDA labeler)

Biogen Inc.

NDC labeler codes: 59627, 64406

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

14Products (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
April 25, 2023NDA215887 Tofersen
QALSODY
Biogen Ma
September 17, 2021BLA761202 Ranibizumab-eqrn
BYOOVIZ
Samsung Bioepis Co Ltd
October 29, 2019NDA211855 Diroximel fumarate
VUMERITY
Biogen
December 23, 2016NDA209531 Nusinersen
SPINRAZA
Biogen
August 15, 2014BLA125499 Peginterferon BETA-1A
PLEGRIDY
Biogen Idec Inc
March 27, 2013NDA204063 Dimethyl fumarate
TECFIDERA
Biogen
November 23, 2004BLA125104 Natalizumab-sztn
TYSABRI
Biogen Idec
May 17, 1996BLA103628 Interferon BETA-1A
AVONEX
Biogen

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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