Quick answers
- What is Genosyl?
- Genosyl is a brand name of Nitric oxide, a prescription medicine. The FDA NDC Directory lists 3 Genosyl products in 1 strength and form.
- Who makes Genosyl?
- Vero Biotech Inc holds the FDA application for Genosyl (NDA202860, approved December 20, 2019).
- Is there a generic or store brand of Genosyl?
- Yes. The FDA NDC Directory lists 1 other product with the same active ingredients, strength and form as a Genosyl product. Ask your pharmacist whether one is right for you.
- Has Genosyl been recalled?
- No recall linked to Genosyl products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Genosyl is
Each Genosyl 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)) | Genosyl | 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
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| NDA202860 | Vero Biotech Inc | December 20, 2019 | 3 |
Companies that list Genosyl
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Genosyl products.
- Vero Biotech, Inc.3 products
Recalls
No recall linked to Genosyl 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.