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Drug company (FDA labeler)

Avyxa Pharma, LLC

NDC labeler code: 83831

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

29Products (NDC)

FDA applications for these products

  • NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
ApprovedApplicationMedicineSponsor
June 24, 2026NDA220436 Fosaprepitant
NAVITRUX
Avyxa Holdings
February 20, 2026NDA220201 Fluorouracil
FAVLYXA
Avyxa Holdings
February 13, 2026NDA220200 Etoposide
AVOPEF
Avyxa Holdings
February 3, 2026NDA220406 Leucovorin calcium
VYKOURA
Avyxa Holdings
August 8, 2025NDA219921 Carboplatin
KYXATA
Avyxa Holdings
July 3, 2025NDA219014 Bendamustine hydrochloride
GOBARDEN
Avyxa Holdings
June 27, 2025NDA219920 Gemcitabine
AVGEMSI
Avyxa Holdings
June 28, 2024NDA210661 Pemetrexed
AXTLE
Avyxa Holdings
June 7, 2023NDA210852 Cyclophosphamide
FRINDOVYX
Avyxa Holdings
November 22, 2022NDA215813 Docetaxel
DOCETAXEL, DOCIVYX
Avyxa Holdings
August 19, 2019NDA210063 Fulvestrant
CLIGAVYX
Avyxa Holdings
March 1, 2016NDA203050 Palonosetron hydrochloride
POSFREA
Avyxa Holdings

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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