Quick answers
- What is Ryzumvi?
- Ryzumvi is a brand name of Phentolamine mesylate, a prescription medicine. The FDA NDC Directory lists 1 Ryzumvi product in 1 strength and form.
- Who makes Ryzumvi?
- Famygen Life Sci holds the FDA application for Ryzumvi (NDA217064, approved September 25, 2023).
- Is there a generic or store brand of Ryzumvi?
- Other products of Phentolamine mesylate are listed with the FDA, but none in exactly the same strength and form as a Ryzumvi product.
- Has Ryzumvi been recalled?
- No recall linked to Ryzumvi products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Ryzumvi is
Each Ryzumvi 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.
Phentolamine mesylate · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| phentolamine mesylate 10 mg/mL solution/ drops (ophthalmic) | Ryzumvi | None listed | — |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Phentolamine mesylate →
FDA approval
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| NDA217064 | Famygen Life Sci | September 25, 2023 | 1 |
Companies that list Ryzumvi
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Ryzumvi products.
- Oyster Point Pharma, Inc.1 product
Recalls
No recall linked to Ryzumvi 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.