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Brand-name prescription medicine

Inomax

Generic name: Nitric oxide

FDA application holder: Mallinckrodt Ireland

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.

Quick answers

What is Inomax?
Inomax is a brand name of Nitric oxide, a prescription medicine. The FDA NDC Directory lists 2 Inomax products in 2 strengths and forms.
Who makes Inomax?
Mallinckrodt Ireland holds the FDA application for Inomax (NDA020845, approved December 23, 1999).
Is there a generic or store brand of Inomax?
Yes. The FDA NDC Directory lists 3 other products with the same active ingredients, strength and form as a Inomax product. Ask your pharmacist whether one is right for you.
Has Inomax been recalled?
No recall linked to Inomax products (by their NDC code or label) appears in the FDA enforcement reports we use.

What Inomax is

Each Inomax 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 0.98 mg/L
gas (respiratory (inhalation))
Inomax 3 products, 1 company DailyMed
nitric oxide 6 mg/L
gas (respiratory (inhalation))
Inomax None listed DailyMed

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

FDA approval

  • NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
FDA applications of Inomax products (Drugs@FDA)
ApplicationHolderFirst approvedProducts
NDA020845Mallinckrodt IrelandDecember 23, 19992

Companies that list Inomax

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

Recalls

No recall linked to Inomax 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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