Quick answers
- What is Xelpros?
- Xelpros is a brand name of Latanoprost, a prescription medicine. The FDA NDC Directory lists 1 Xelpros product in 1 strength and form.
- Who makes Xelpros?
- Sun Pharm holds the FDA application for Xelpros (NDA206185, approved September 12, 2018).
- Is there a generic or store brand of Xelpros?
- Other products of Latanoprost are listed with the FDA, but none in exactly the same strength and form as a Xelpros product.
- Has Xelpros been recalled?
- FDA enforcement reports list 1 recall of Xelpros products; the newest started April 22, 2024. A recall usually concerns specific lots, not every product.
What Xelpros is
Each Xelpros 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.
Latanoprost · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| latanoprost 0.05 mg/mL solution/ drops (ophthalmic, topical) | Xelpros | None listed | DailyMed |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Latanoprost →
FDA approval
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| NDA206185 | Sun Pharm | September 12, 2018 | 1 |
Companies that list Xelpros
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Xelpros products.
- Sun Pharmaceutical Industries, Inc.1 product
Recalls
From FDA enforcement reports, matched by the product’s NDC code or label. A recall usually covers specific lots: check the lot number on your package and ask your pharmacist. Do not stop a medicine on your own.
-
April 22, 2024 · Class III · Ongoing · D-0502-2024
Failed Release Testing: Out of specification for particulate matter test.
Xelpros (latanoprost ophthalmic emulsion) 0.005%, 125mcg/2.5mL, 2.5 mL bottle, Rx only, Manufactured by: Sun Pharmaceutical Ind. Ltd., India., NDC 47335-317-90 — SUN PHARMACEUTICAL INDUSTRIES INC
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.