Quick answers
- What is Membraneblue?
- Membraneblue is a brand name of Trypan blue, a prescription medicine. The FDA NDC Directory lists 1 Membraneblue product in 1 strength and form.
- Who makes Membraneblue?
- Dorc holds the FDA application for Membraneblue (NDA022278, approved February 20, 2009).
- Is there a generic or store brand of Membraneblue?
- Other products of Trypan blue are listed with the FDA, but none in exactly the same strength and form as a Membraneblue product.
- Has Membraneblue been recalled?
- No recall linked to Membraneblue products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Membraneblue is
Each Membraneblue 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.
Trypan blue · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| trypan blue 0.75 mg/0.5 mL injection, solution (intraocular, ophthalmic) | Membraneblue | None listed | DailyMed |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Trypan blue →
FDA approval
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| NDA022278 | Dorc | February 20, 2009 | 1 |
Companies that list Membraneblue
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Membraneblue products.
Recalls
No recall linked to Membraneblue 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.