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 form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| 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.
| Application | Holder | First approved | Products |
|---|---|---|---|
| NDA020845 | Mallinckrodt Ireland | December 23, 1999 | 2 |
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.
- INO Therapeutics LLC2 products
Recalls
No recall linked to Inomax products (by their NDC code or label) appears in the FDA enforcement reports.
Sources
- NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug labeling (SPL, openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
- 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.