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Drug company (FDA labeler)

EMD Serono, Inc.

NDC labeler code: 44087

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)

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
February 3, 2021NDA214096 Tepotinib hydrochloride
TEPMETKO
Emd Serono Inc
March 29, 2019NDA022561 Cladribine
MAVENCLAD
Emd Serono Inc
March 23, 2017BLA761049 Avelumab
BAVENCIO
Emd Serono Inc
May 25, 2004BLA021684 Follitropin
GONAL-F RFF REDI-JECT
Emd Serono
March 7, 2002BLA103780 Interferon BETA-1A
REBIF
Serono Inc
September 20, 2000BLA021149 Choriogonadotropin alfa
OVIDREL
Emd Serono

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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