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Drug company (FDA labeler)

NexAir, LLC

NDC labeler code: 12213

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

10Products (NDC)

Prescription medicines

FDA applications for these products

  • NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
ApprovedApplicationMedicineSponsor
July 18, 2020NDA215007 Carbon dioxide
CARBON DIOXIDE, USP
Nexair LLC
February 20, 2016NDA209033 Helium
HELIUM, USP
Nexair LLC
September 3, 2013NDA206009 Nitrous oxide
NITROUS OXIDE, USP
Nitrous Oxide Corp
July 23, 2013NDA205859 Air
MEDICAL AIR, USP
Nexair
July 23, 2013NDA205865 Oxygen
OXYGEN, USP
Air Products and Chemicals Inc
July 21, 2013NDA205849 Oxygen
OXYGEN, USP
Praxair Inc
July 21, 2013NDA205850 Nitrogen
NITROGEN, NF
Praxair Inc

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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