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Brand-name prescription medicine

Suprane

Generic name: Desflurane

FDA application holder: Baxter Hlthcare

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 Suprane?
Suprane is a brand name of Desflurane, a prescription medicine. The FDA NDC Directory lists 4 Suprane products in 1 strength and form.
Who makes Suprane?
Baxter Hlthcare holds the FDA application for Suprane (NDA020118, approved September 18, 1992). 1 other company (repackagers or distributors) also list Suprane products.
Is there a generic or store brand of Suprane?
Yes. The FDA NDC Directory lists 1 other product with the same active ingredients, strength and form as a Suprane product, 1 of them generic. Ask your pharmacist whether one is right for you.
Has Suprane been recalled?
No recall linked to Suprane products (by their NDC code or label) appears in the FDA enforcement reports we use.

What Suprane is

Each Suprane 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.

Desflurane · prescription medicine

Strength and formProduct namesSame medicine, other namesLabel
desflurane 240 mL/240 mL
liquid (respiratory (inhalation))
Suprane 1 product, 1 company DailyMed

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

FDA approval

  • NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
FDA applications of Suprane products (Drugs@FDA)
ApplicationHolderFirst approvedProducts
NDA020118Baxter HlthcareSeptember 18, 19924

Companies that list Suprane

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

Recalls

No recall linked to Suprane 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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