Quick answers
- What is Varibar Thin Honey?
- Varibar Thin Honey is a brand name of Barium sulfate, a prescription medicine. The FDA NDC Directory lists 1 Varibar Thin Honey product in 1 strength and form.
- Who makes Varibar Thin Honey?
- Bracco holds the FDA application for Varibar Thin Honey (NDA208143, approved January 15, 2016).
- Is there a generic or store brand of Varibar Thin Honey?
- Yes. The FDA NDC Directory lists 3 other products with the same active ingredients, strength and form as a Varibar Thin Honey product. Ask your pharmacist whether one is right for you.
- Has Varibar Thin Honey been recalled?
- No recall linked to Varibar Thin Honey products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Varibar Thin Honey is
Each Varibar Thin Honey 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 form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| barium sulfate 400 mg/mL suspension (oral) | Varibar Thin Honey | 3 products, 1 company | 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.
| Application | Holder | First approved | Products |
|---|---|---|---|
| NDA208143 | Bracco | January 15, 2016 | 1 |
Companies that list Varibar Thin Honey
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Varibar Thin Honey products.
- E-Z-EM Canada Inc1 product
Recalls
No recall linked to Varibar Thin Honey products (by their NDC code or label) appears in the FDA enforcement reports.
Sources
- NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug labeling (SPL, openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
- 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.