Quick answers
- What is Valstar?
- Valstar is a brand name of Valrubicin intravesical solution, a prescription medicine. The FDA NDC Directory lists 1 Valstar product in 1 strength and form.
- Who makes Valstar?
- Endo Operations holds the FDA application for Valstar (NDA020892, approved September 25, 1998).
- Is there a generic or store brand of Valstar?
- Yes. The FDA NDC Directory lists 1 other product with the same active ingredients, strength and form as a Valstar product, 1 of them generic. Ask your pharmacist whether one is right for you.
- Has Valstar been recalled?
- No recall linked to Valstar products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Valstar is
Each Valstar 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.
Valrubicin intravesical solution · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| valrubicin 40 mg/mL solution, concentrate (intravesical) | Valstar | 1 product, 1 company | DailyMed |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Valrubicin intravesical solution →
FDA approval
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| NDA020892 | Endo Operations | September 25, 1998 | 1 |
Companies that list Valstar
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Valstar products.
- Endo USA, Inc.1 product
Recalls
No recall linked to Valstar 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.