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Brand-name prescription medicine

Iopidine 1%

Generic name: Apraclonidine hydrochloride ophthalmic solution

FDA application holder: Harrow Eye

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 Iopidine 1%?
Iopidine 1% is a brand name of Apraclonidine hydrochloride ophthalmic solution, a prescription medicine. The FDA NDC Directory lists 1 Iopidine 1% product in 1 strength and form.
Who makes Iopidine 1%?
Harrow Eye holds the FDA application for Iopidine 1% (NDA019779, approved December 31, 1987).
Is there a generic or store brand of Iopidine 1%?
Other products of Apraclonidine hydrochloride ophthalmic solution are listed with the FDA, but none in exactly the same strength and form as a Iopidine 1% product.
Has Iopidine 1% been recalled?
No recall linked to Iopidine 1% products (by their NDC code or label) appears in the FDA enforcement reports we use.

What Iopidine 1% is

Each Iopidine 1% 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.

Apraclonidine hydrochloride ophthalmic solution · prescription medicine

Strength and formProduct namesSame medicine, other namesLabel
apraclonidine hydrochloride 10 mg/mL
solution/ drops (ophthalmic)
Iopidine 1% None listed DailyMed

Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Apraclonidine hydrochloride ophthalmic solution →

FDA approval

  • NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
FDA applications of Iopidine 1% products (Drugs@FDA)
ApplicationHolderFirst approvedProducts
NDA019779Harrow EyeDecember 31, 19871

Companies that list Iopidine 1%

The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Iopidine 1% products.

Recalls

No recall linked to Iopidine 1% 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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