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Brand-name prescription medicine

Tridacaine III

Generic name: Lidocaine

FDA application holder: Ibsa

Strengths and generic versions Official label

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.

At a glance

1Strengths and forms
36Same medicine, other names
2020FDA approval
0Recalls (FDA reports)

Quick answers

What is Tridacaine III?
Tridacaine III is a brand name of Lidocaine, a prescription medicine. The FDA NDC Directory lists 1 Tridacaine III product in 1 strength and form.
Who makes Tridacaine III?
Ibsa holds the FDA application for Tridacaine III (ANDA209190, approved April 30, 2020).
Is there a generic or store brand of Tridacaine III?
Yes. The FDA NDC Directory lists 36 other products with the same active ingredients, strength and form as a Tridacaine III product, 36 of them generic. Ask your pharmacist whether one is right for you.
Has Tridacaine III been recalled?
No recall linked to Tridacaine III products (by their NDC code or label) appears in the FDA enforcement reports we use.

What Tridacaine III is

Each Tridacaine III 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.

Lidocaine · prescription medicine

Strength and formProduct namesSame medicine, other namesLabel
lidocaine 5%
patch (topical)		 Tridacaine III 36 products, 20 companies DailyMed

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

FDA approval

  • ANDA: Abbreviated New Drug Application: how a generic version is approved.
FDA applications of Tridacaine III products (Drugs@FDA)
ApplicationHolderFirst approvedProducts
ANDA209190IbsaApril 30, 20201

Companies that list Tridacaine III

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

Recalls

No recall linked to Tridacaine III 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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