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Brand-name prescription medicine

Noxivent 102

Generic name: Nitric oxide

FDA application holder: Vero Biotech Inc

Strengths and generic versions Official label

Official data, not advice

Everything here comes from the U.S. Food and Drug Administration (FDA): the NDC Directory, Drugs@FDA, the official labels and recall reports; pharmacy costs come from the Centers for Medicare & Medicaid Services (CMS). Each fact shows its source and date.

This page is not medical advice. Talk to your doctor or pharmacist before you start, stop or switch any medicine, including a switch between a brand and a generic.

In an emergency, call 911. If someone may have taken too much of a medicine, call Poison Help: 1‑800‑222‑1222.

At a glance

1Strengths and forms
1Same medicine, other names
2018FDA approval
0Recalls (FDA reports)

Quick answers

What is Noxivent 102?
Noxivent 102 is a brand name of Nitric oxide, a prescription medicine. The FDA NDC Directory lists 1 Noxivent 102 product in 1 strength and form.
Who makes Noxivent 102?
Vero Biotech Inc holds the FDA application for Noxivent 102 (ANDA207141, approved October 2, 2018).
Is there a generic or store brand of Noxivent 102?
Yes. The FDA NDC Directory lists 1 other product with the same active ingredients, strength and form as a Noxivent 102 product, 1 of them generic. Ask your pharmacist whether one is right for you.
Has Noxivent 102 been recalled?
No recall linked to Noxivent 102 products (by their NDC code or label) appears in the FDA enforcement reports we use.

What Noxivent 102 is

Each Noxivent 102 product as listed in the FDA NDC Directory, by active ingredient, strength and form, with its official label. “Same medicine, other names” counts the other products with exactly the same active ingredients, strength and form (generic versions, store brands and other brands); inactive ingredients can differ.

Nitric oxide · prescription medicine

Strength and formProduct namesSame medicine, other namesLabel
nitric oxide 800 mg/L
gas (respiratory (inhalation))		 Noxivent 102 1 product, 1 company DailyMed

Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Nitric oxide →

FDA approval

  • ANDA: Abbreviated New Drug Application: how a generic version is approved.
FDA applications of Noxivent 102 products (Drugs@FDA)
ApplicationHolderFirst approvedProducts
ANDA207141Vero Biotech IncOctober 2, 20181

Companies that list Noxivent 102

The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Noxivent 102 products.

Recalls

No recall linked to Noxivent 102 products (by their NDC code or label) 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 labeling (SPL, openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  4. Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
  5. NADAC (National Average Drug Acquisition Cost) 2026 — Centers for Medicare & Medicaid Services (CMS), data.medicaid.gov, list of November 4, 2026, retrieved November 7, 2026

Which names get a brand page: a name the NDC Directory lists for a medicine, held by one company (the FDA application holder, or the company named on most of its products), that is not just a description, and that is not the only product of its medicine.

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