Quick answers
- What is iDose TR?
- iDose TR is a brand name of Travoprost ophthalmic solution, a prescription medicine. The FDA NDC Directory lists 1 iDose TR product in 1 strength and form.
- Who makes iDose TR?
- Glaukos holds the FDA application for iDose TR (NDA218010, approved December 13, 2023).
- Is there a generic or store brand of iDose TR?
- Other products of Travoprost ophthalmic solution are listed with the FDA, but none in exactly the same strength and form as a iDose TR product.
- Has iDose TR been recalled?
- No recall linked to iDose TR products (by their NDC code or label) appears in the FDA enforcement reports we use.
What iDose TR is
Each iDose TR 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.
Travoprost ophthalmic solution · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| travoprost 75 ug implant (intracameral) | iDose TR | None listed | DailyMed |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Travoprost ophthalmic solution →
FDA approval
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| NDA218010 | Glaukos | December 13, 2023 | 1 |
Companies that list iDose TR
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of iDose TR products.
- Glaukos Corporation1 product
Recalls
No recall linked to iDose TR 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.