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Brand-name prescription medicine

Ak-Fluor

Generic name: Fluorescein (fluorescein sodium)

FDA application holder: Long Grove Pharms

Official data, not advice

Everything here comes from the U.S. Food and Drug Administration (FDA): the NDC Directory, Drugs@FDA, the official labels and recall reports; pharmacy costs come from the Centers for Medicare & Medicaid Services (CMS). Each fact shows its source and date.

This page is not medical advice. Talk to your doctor or pharmacist before you start, stop or switch any medicine, including a switch between a brand and a generic.

In an emergency, call 911. If someone may have taken too much of a medicine, call Poison Help: 1‑800‑222‑1222.

Quick answers

What is Ak-Fluor?
Ak-Fluor is a brand name of Fluorescein (fluorescein sodium), a prescription medicine. The FDA NDC Directory lists 1 Ak-Fluor product in 1 strength and form.
Who makes Ak-Fluor?
Long Grove Pharms holds the FDA application for Ak-Fluor (NDA022186, approved August 8, 2008).
Is there a generic or store brand of Ak-Fluor?
Yes. The FDA NDC Directory lists 4 other products with the same active ingredients, strength and form as a Ak-Fluor product, 3 of them generic. Ask your pharmacist whether one is right for you.
Has Ak-Fluor been recalled?
No recall linked to Ak-Fluor products (by their NDC code or label) appears in the FDA enforcement reports we use.

What Ak-Fluor is

Each Ak-Fluor 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.

Fluorescein (fluorescein sodium) · prescription medicine

Strength and formProduct namesSame medicine, other namesLabel
fluorescein sodium 100 mg/mL
injection (intravenous)
Ak-Fluor 4 products, 4 companies DailyMed

Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Fluorescein (fluorescein sodium) →

FDA approval

  • NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
FDA applications of Ak-Fluor products (Drugs@FDA)
ApplicationHolderFirst approvedProducts
NDA022186Long Grove PharmsAugust 8, 20081

Companies that list Ak-Fluor

The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Ak-Fluor products.

Recalls

No recall linked to Ak-Fluor products (by their NDC code or label) appears in the FDA enforcement reports.

Sources

  1. NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  2. Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  3. Drug labeling (SPL, openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  4. Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
  5. 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.

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