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Brand-name prescription medicine

Varibar Thin Liquid

Generic name: Barium sulfate

FDA application holder: Bracco

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 Varibar Thin Liquid?
Varibar Thin Liquid is a brand name of Barium sulfate, a prescription medicine. The FDA NDC Directory lists 1 Varibar Thin Liquid product in 1 strength and form.
Who makes Varibar Thin Liquid?
Bracco holds the FDA application for Varibar Thin Liquid (NDA208036, approved January 11, 2016).
Is there a generic or store brand of Varibar Thin Liquid?
Other products of Barium sulfate are listed with the FDA, but none in exactly the same strength and form as a Varibar Thin Liquid product.
Has Varibar Thin Liquid been recalled?
No recall linked to Varibar Thin Liquid products (by their NDC code or label) appears in the FDA enforcement reports we use.

What Varibar Thin Liquid is

Each Varibar Thin Liquid 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.

Barium sulfate · prescription medicine

Strength and formProduct namesSame medicine, other namesLabel
barium sulfate 81%
powder, for suspension (oral)
Varibar Thin Liquid None listed DailyMed

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

FDA approval

  • NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
FDA applications of Varibar Thin Liquid products (Drugs@FDA)
ApplicationHolderFirst approvedProducts
NDA208036BraccoJanuary 11, 20161

Companies that list Varibar Thin Liquid

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

Recalls

No recall linked to Varibar Thin Liquid 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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